A Highly Polymorphic Poly‐Glutamine Stretch in the Potassium Channel KCNN3 in Migraine
Identifieur interne : 000B13 ( Istex/Corpus ); précédent : 000B12; suivant : 000B14A Highly Polymorphic Poly‐Glutamine Stretch in the Potassium Channel KCNN3 in Migraine
Auteurs : Rainald Mössner ; Annette Weichselbaum ; Martin Marziniak ; Christine M. Freitag ; Klaus-Peter Lesch ; Claudia Sommer ; Jobst MeyerSource :
- Headache: The Journal of Head and Face Pain [ 0017-8748 ] ; 2005-02.
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Abstract
Objective.—The present study is designed to further elucidate the molecular genetic basis of migraine with and without aura. Background.—Migraine is a common disease of as yet unknown etiology. Interest in ion channels in migraine has been spurred by molecular genetic findings in familial hemiplegic migraine, since familial hemiplegic migraine type 1 is caused by mutations in the calcium channel gene CACNA1A. Methods.—Given this role of ion channels in migraine, we assessed the potassium channel KCNN3 as a candidate gene for common migraine. We analyzed the highly polymorphic repeat region coding for a poly‐glutamine stretch, which constitutes part of the cytoplasmic tail of the channel protein. Results.—We found an excess of the allele coding for 15 poly‐glutamines in migraine patients. Conclusions.—The potassium channel KCNN3 may thus be of pathophysiological importance in migraine with and without aura.
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DOI: 10.1111/j.1526-4610.2005.05027.x
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ISTEX:A765B8E841FABF919A2522DCE0BC663DC69DAF33Le document en format XML
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Freitag</name></author><author><name sortKey="Lesch, Klaus Eter" sort="Lesch, Klaus Eter" uniqKey="Lesch K" first="Klaus-Peter" last="Lesch">Klaus-Peter Lesch</name></author><author><name sortKey="Sommer, Claudia" sort="Sommer, Claudia" uniqKey="Sommer C" first="Claudia" last="Sommer">Claudia Sommer</name></author><author><name sortKey="Meyer, Jobst" sort="Meyer, Jobst" uniqKey="Meyer J" first="Jobst" last="Meyer">Jobst Meyer</name></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:A765B8E841FABF919A2522DCE0BC663DC69DAF33</idno><date when="2005" year="2005">2005</date><idno type="doi">10.1111/j.1526-4610.2005.05027.x</idno><idno type="url">https://api.istex.fr/document/A765B8E841FABF919A2522DCE0BC663DC69DAF33/fulltext/pdf</idno><idno type="wicri:Area/Istex/Corpus">000B13</idno><idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">000B13</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">A Highly Polymorphic Poly‐Glutamine Stretch in the Potassium Channel KCNN3 in Migraine</title><author><name sortKey="Mossner, Rainald" sort="Mossner, Rainald" uniqKey="Mossner R" first="Rainald" last="Mössner">Rainald Mössner</name></author><author><name sortKey="Weichselbaum, Annette" sort="Weichselbaum, Annette" uniqKey="Weichselbaum A" first="Annette" last="Weichselbaum">Annette Weichselbaum</name></author><author><name sortKey="Marziniak, Martin" sort="Marziniak, Martin" uniqKey="Marziniak M" first="Martin" last="Marziniak">Martin Marziniak</name></author><author><name sortKey="Freitag, Christine M" sort="Freitag, Christine M" uniqKey="Freitag C" first="Christine M" last="Freitag">Christine M. Freitag</name></author><author><name sortKey="Lesch, Klaus Eter" sort="Lesch, Klaus Eter" uniqKey="Lesch K" first="Klaus-Peter" last="Lesch">Klaus-Peter Lesch</name></author><author><name sortKey="Sommer, Claudia" sort="Sommer, Claudia" uniqKey="Sommer C" first="Claudia" last="Sommer">Claudia Sommer</name></author><author><name sortKey="Meyer, Jobst" sort="Meyer, Jobst" uniqKey="Meyer J" first="Jobst" last="Meyer">Jobst Meyer</name></author></analytic><monogr></monogr><series><title level="j">Headache: The Journal of Head and Face Pain</title><idno type="ISSN">0017-8748</idno><idno type="eISSN">1526-4610</idno><imprint><publisher>Blackwell Science Inc</publisher><pubPlace>350 Main Street , Malden , MA 02148 , USA</pubPlace><date type="published" when="2005-02">2005-02</date><biblScope unit="volume">45</biblScope><biblScope unit="issue">2</biblScope><biblScope unit="page" from="132">132</biblScope><biblScope unit="page" to="136">136</biblScope></imprint><idno type="ISSN">0017-8748</idno></series><idno type="istex">A765B8E841FABF919A2522DCE0BC663DC69DAF33</idno><idno type="DOI">10.1111/j.1526-4610.2005.05027.x</idno><idno type="ArticleID">HEAD05027</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0017-8748</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>KCNN3</term><term>aura</term><term>migraine</term><term>poly‐glutamine</term><term>potassium channel</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Objective.—The present study is designed to further elucidate the molecular genetic basis of migraine with and without aura. Background.—Migraine is a common disease of as yet unknown etiology. Interest in ion channels in migraine has been spurred by molecular genetic findings in familial hemiplegic migraine, since familial hemiplegic migraine type 1 is caused by mutations in the calcium channel gene CACNA1A. Methods.—Given this role of ion channels in migraine, we assessed the potassium channel KCNN3 as a candidate gene for common migraine. We analyzed the highly polymorphic repeat region coding for a poly‐glutamine stretch, which constitutes part of the cytoplasmic tail of the channel protein. Results.—We found an excess of the allele coding for 15 poly‐glutamines in migraine patients. Conclusions.—The potassium channel KCNN3 may thus be of pathophysiological importance in migraine with and without aura.</div></front></TEI><istex><corpusName>wiley</corpusName><author><json:item><name>Rainald Mössner MD</name></json:item><json:item><name>Annette Weichselbaum MD</name></json:item><json:item><name>Martin Marziniak MD</name></json:item><json:item><name>Christine M Freitag MD</name></json:item><json:item><name>Klaus‐Peter Lesch MD</name></json:item><json:item><name>Claudia Sommer MD</name></json:item><json:item><name>Jobst Meyer PhD</name></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>migraine</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>aura</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>potassium channel</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>KCNN3</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>poly‐glutamine</value></json:item></subject><articleId><json:string>HEAD05027</json:string></articleId><language><json:string>eng</json:string></language><originalGenre><json:string>article</json:string></originalGenre><abstract>Objective.—The present study is designed to further elucidate the molecular genetic basis of migraine with and without aura. Background.—Migraine is a common disease of as yet unknown etiology. Interest in ion channels in migraine has been spurred by molecular genetic findings in familial hemiplegic migraine, since familial hemiplegic migraine type 1 is caused by mutations in the calcium channel gene CACNA1A. Methods.—Given this role of ion channels in migraine, we assessed the potassium channel KCNN3 as a candidate gene for common migraine. We analyzed the highly polymorphic repeat region coding for a poly‐glutamine stretch, which constitutes part of the cytoplasmic tail of the channel protein. Results.—We found an excess of the allele coding for 15 poly‐glutamines in migraine patients. Conclusions.—The potassium channel KCNN3 may thus be of pathophysiological importance in migraine with and without aura.</abstract><qualityIndicators><score>4.46</score><pdfVersion>1.3</pdfVersion><pdfPageSize>594 x 783 pts</pdfPageSize><refBibsNative>true</refBibsNative><abstractCharCount>919</abstractCharCount><pdfWordCount>2840</pdfWordCount><pdfCharCount>17812</pdfCharCount><pdfPageCount>5</pdfPageCount><abstractWordCount>135</abstractWordCount></qualityIndicators><title>A Highly Polymorphic Poly‐Glutamine Stretch in the Potassium Channel KCNN3 in Migraine</title><refBibs><json:item><author><json:item><name>N Breslau</name></json:item><json:item><name>BK Rasmussen</name></json:item></author><host><volume>56</volume><pages><last>12</last><first>4</first></pages><author></author><title>Neurology</title></host><title>The impact of migraine: epidemiology, risk factors, and co‐morbidities</title></json:item><json:item><author><json:item><name>P 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The spreading depression theory</title></json:item></refBibs><genre><json:string>article</json:string></genre><host><volume>45</volume><publisherId><json:string>HEAD</json:string></publisherId><pages><total>5</total><last>136</last><first>132</first></pages><issn><json:string>0017-8748</json:string></issn><issue>2</issue><genre><json:string>journal</json:string></genre><language><json:string>unknown</json:string></language><eissn><json:string>1526-4610</json:string></eissn><title>Headache: The Journal of Head and Face Pain</title><doi><json:string>10.1111/(ISSN)1526-4610</json:string></doi></host><categories><wos><json:string>science</json:string><json:string>clinical neurology</json:string></wos><scienceMetrix><json:string>health sciences</json:string><json:string>clinical medicine</json:string><json:string>neurology & neurosurgery</json:string></scienceMetrix></categories><publicationDate>2005</publicationDate><copyrightDate>2005</copyrightDate><doi><json:string>10.1111/j.1526-4610.2005.05027.x</json:string></doi><id>A765B8E841FABF919A2522DCE0BC663DC69DAF33</id><score>0.027397353</score><fulltext><json:item><extension>pdf</extension><original>true</original><mimetype>application/pdf</mimetype><uri>https://api.istex.fr/document/A765B8E841FABF919A2522DCE0BC663DC69DAF33/fulltext/pdf</uri></json:item><json:item><extension>zip</extension><original>false</original><mimetype>application/zip</mimetype><uri>https://api.istex.fr/document/A765B8E841FABF919A2522DCE0BC663DC69DAF33/fulltext/zip</uri></json:item><istex:fulltextTEI uri="https://api.istex.fr/document/A765B8E841FABF919A2522DCE0BC663DC69DAF33/fulltext/tei"><teiHeader><fileDesc><titleStmt><title level="a" type="main" xml:lang="en">A Highly Polymorphic Poly‐Glutamine Stretch in the Potassium Channel KCNN3 in Migraine</title></titleStmt><publicationStmt><authority>ISTEX</authority><publisher>Blackwell Science Inc</publisher><pubPlace>350 Main Street , Malden , MA 02148 , USA</pubPlace><availability><p>WILEY</p></availability><date>2005</date></publicationStmt><sourceDesc><biblStruct type="inbook"><analytic><title level="a" type="main" xml:lang="en">A Highly Polymorphic Poly‐Glutamine Stretch in the Potassium Channel KCNN3 in Migraine</title><author xml:id="author-1"><persName><forename type="first">Rainald</forename><surname>Mössner</surname></persName><roleName type="degree">MD</roleName></author><author xml:id="author-2"><persName><forename type="first">Annette</forename><surname>Weichselbaum</surname></persName><roleName type="degree">MD</roleName></author><author xml:id="author-3"><persName><forename type="first">Martin</forename><surname>Marziniak</surname></persName><roleName type="degree">MD</roleName></author><author xml:id="author-4"><persName><forename type="first">Christine M</forename><surname>Freitag</surname></persName><roleName type="degree">MD</roleName></author><author xml:id="author-5"><persName><forename type="first">Klaus‐Peter</forename><surname>Lesch</surname></persName><roleName type="degree">MD</roleName></author><author xml:id="author-6"><persName><forename type="first">Claudia</forename><surname>Sommer</surname></persName><roleName type="degree">MD</roleName></author><author xml:id="author-7"><persName><forename type="first">Jobst</forename><surname>Meyer</surname></persName><roleName type="degree">PhD</roleName></author></analytic><monogr><title level="j">Headache: The Journal of Head and Face Pain</title><idno type="pISSN">0017-8748</idno><idno type="eISSN">1526-4610</idno><idno type="DOI">10.1111/(ISSN)1526-4610</idno><imprint><publisher>Blackwell Science Inc</publisher><pubPlace>350 Main Street , Malden , MA 02148 , USA</pubPlace><date type="published" when="2005-02"></date><biblScope unit="volume">45</biblScope><biblScope unit="issue">2</biblScope><biblScope unit="page" from="132">132</biblScope><biblScope unit="page" to="136">136</biblScope></imprint></monogr><idno type="istex">A765B8E841FABF919A2522DCE0BC663DC69DAF33</idno><idno type="DOI">10.1111/j.1526-4610.2005.05027.x</idno><idno type="ArticleID">HEAD05027</idno></biblStruct></sourceDesc></fileDesc><profileDesc><creation><date>2005</date></creation><langUsage><language ident="en">en</language></langUsage><abstract xml:lang="en"><p>Objective.—The present study is designed to further elucidate the molecular genetic basis of migraine with and without aura. Background.—Migraine is a common disease of as yet unknown etiology. Interest in ion channels in migraine has been spurred by molecular genetic findings in familial hemiplegic migraine, since familial hemiplegic migraine type 1 is caused by mutations in the calcium channel gene CACNA1A. Methods.—Given this role of ion channels in migraine, we assessed the potassium channel KCNN3 as a candidate gene for common migraine. We analyzed the highly polymorphic repeat region coding for a poly‐glutamine stretch, which constitutes part of the cytoplasmic tail of the channel protein. Results.—We found an excess of the allele coding for 15 poly‐glutamines in migraine patients. Conclusions.—The potassium channel KCNN3 may thus be of pathophysiological importance in migraine with and without aura.</p></abstract><textClass xml:lang="en"><keywords scheme="keyword"><list><head>keywords</head><item><term>migraine</term></item><item><term>aura</term></item><item><term>potassium channel</term></item><item><term>KCNN3</term></item><item><term>poly‐glutamine</term></item></list></keywords></textClass></profileDesc><revisionDesc><change when="2005-02">Published</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/document/A765B8E841FABF919A2522DCE0BC663DC69DAF33/fulltext/txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Wiley, elements deleted: body"><istex:xmlDeclaration>version="1.0" encoding="UTF-8" standalone="yes"</istex:xmlDeclaration><istex:document><component version="2.0" type="serialArticle" xml:lang="en"><header><publicationMeta level="product"><publisherInfo><publisherName>Blackwell Science Inc</publisherName><publisherLoc> 350 Main Street , Malden , MA 02148 , USA </publisherLoc></publisherInfo><doi origin="wiley" registered="yes">10.1111/(ISSN)1526-4610</doi><issn type="print">0017-8748</issn><issn type="electronic">1526-4610</issn><idGroup><id type="product" value="HEAD"></id><id type="publisherDivision" value="ST"></id></idGroup><titleGroup><title type="main" sort="HEADACHE JOURNAL HEAD FACE PAIN">Headache: The Journal of Head and Face Pain</title></titleGroup></publicationMeta><publicationMeta level="part" position="02002"><doi origin="wiley">10.1111/hed.2005.45.issue-2</doi><numberingGroup><numbering type="journalVolume" number="45">45</numbering><numbering type="journalIssue" number="2">2</numbering></numberingGroup><coverDate startDate="2005-02">February 2005</coverDate></publicationMeta><publicationMeta level="unit" type="article" position="7" status="forIssue"><doi origin="wiley">10.1111/j.1526-4610.2005.05027.x</doi><idGroup><id type="unit" value="HEAD05027"></id><id type="supplier" value="hed05027"></id></idGroup><countGroup><count type="pageTotal" number="5"></count></countGroup><titleGroup><title type="tocHeading1">Research Submissions</title></titleGroup><eventGroup><event type="firstOnline" date="2005-02-10"></event><event type="publishedOnlineFinalForm" date="2005-02-10"></event><event type="xmlConverted" agent="Converter:BPG_TO_WML3G version:2.3.6 mode:FullText" date="2010-04-27"></event><event type="xmlConverted" agent="Converter:WILEY_ML3G_TO_WILEY_ML3GV2 version:3.8.8" date="2014-01-26"></event><event type="xmlConverted" agent="Converter:WML3G_To_WML3G version:4.1.7 mode:FullText,remove_FC" date="2014-10-24"></event></eventGroup><numberingGroup><numbering type="pageFirst" number="132">132</numbering><numbering type="pageLast" number="136">136</numbering></numberingGroup><correspondenceTo>Address all correspondence to Dr. R. Mössner, Department of Psychiatry and Psychotherapy, University of Würzburg, Germany.</correspondenceTo><linkGroup><link type="toTypesetVersion" href="file:HEAD.HEAD05027.pdf"></link></linkGroup></publicationMeta><contentMeta><unparsedEditorialHistory>Accepted for publication May 19, 2004.</unparsedEditorialHistory><countGroup><count type="figureTotal" number="1"></count><count type="tableTotal" number="0"></count><count type="formulaTotal" number="0"></count><count type="referenceTotal" number="26"></count><count type="linksCrossRef" number="31"></count></countGroup><titleGroup><title type="main">A Highly Polymorphic Poly‐Glutamine Stretch in the Potassium Channel KCNN3 in Migraine</title></titleGroup><creators><creator creatorRole="author" xml:id="cr1"><personName><givenNames>Rainald</givenNames><familyName>Mössner</familyName><degrees>MD</degrees></personName></creator><creator creatorRole="author" xml:id="cr2"><personName><givenNames>Annette</givenNames><familyName>Weichselbaum</familyName><degrees>MD</degrees></personName></creator><creator creatorRole="author" xml:id="cr3"><personName><givenNames>Martin</givenNames><familyName>Marziniak</familyName><degrees>MD</degrees></personName></creator><creator creatorRole="author" xml:id="cr4"><personName><givenNames>Christine M</givenNames><familyName>Freitag</familyName><degrees>MD</degrees></personName></creator><creator creatorRole="author" xml:id="cr5"><personName><givenNames>Klaus‐Peter</givenNames><familyName>Lesch</familyName><degrees>MD</degrees></personName></creator><creator creatorRole="author" xml:id="cr6"><personName><givenNames>Claudia</givenNames><familyName>Sommer</familyName><degrees>MD</degrees></personName></creator><creator creatorRole="author" xml:id="cr7"><personName><givenNames>Jobst</givenNames><familyName>Meyer</familyName><degrees>PhD</degrees></personName></creator></creators><keywordGroup xml:lang="en"><keyword xml:id="k1">migraine</keyword><keyword xml:id="k2">aura</keyword><keyword xml:id="k3">potassium channel</keyword><keyword xml:id="k4">KCNN3</keyword><keyword xml:id="k5">poly‐glutamine</keyword></keywordGroup><abstractGroup><abstract type="main" xml:lang="en"><p>Objective.—The present study is designed to further elucidate the molecular genetic basis of migraine with and without aura.</p><p>Background.—Migraine is a common disease of as yet unknown etiology. Interest in ion channels in migraine has been spurred by molecular genetic findings in familial hemiplegic migraine, since familial hemiplegic migraine type 1 is caused by mutations in the calcium channel gene CACNA1A.</p><p>Methods.—Given this role of ion channels in migraine, we assessed the potassium channel KCNN3 as a candidate gene for common migraine. We analyzed the highly polymorphic repeat region coding for a poly‐glutamine stretch, which constitutes part of the cytoplasmic tail of the channel protein.</p><p>Results.—We found an excess of the allele coding for 15 poly‐glutamines in migraine patients.</p><p>Conclusions.—The potassium channel KCNN3 may thus be of pathophysiological importance in migraine with and without aura.</p><!-- (Headache 2005;45:132-136)
</abstractGroup></contentMeta><noteGroup><note xml:id="n-fnt-1" numbered="no"><p>From the Department of Psychiatry, University of Würzburg, Würzburg, Germany (Drs. Mössner, Weichselbaum, and Lesch); Department of Neurology, University of Würzburg, Würzburg, Germany (Drs. Marziniak and Sommer); Department of Child and Adolescent Psychiatry, University Hospital Saarland, Homburg, Germany (Dr. Freitag); and University of Trier, Department of Neuro‐Behavioral Genetics, Trier, Germany (Dr. Meyer).</p></note></noteGroup></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>A Highly Polymorphic Poly‐Glutamine Stretch in the Potassium Channel KCNN3 in Migraine</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>A Highly Polymorphic Poly‐Glutamine Stretch in the Potassium Channel KCNN3 in Migraine</title></titleInfo><name type="personal"><namePart type="given">Rainald</namePart><namePart type="family">Mössner</namePart><namePart type="termsOfAddress">MD</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Annette</namePart><namePart type="family">Weichselbaum</namePart><namePart type="termsOfAddress">MD</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Martin</namePart><namePart type="family">Marziniak</namePart><namePart type="termsOfAddress">MD</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Christine M</namePart><namePart type="family">Freitag</namePart><namePart type="termsOfAddress">MD</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Klaus‐Peter</namePart><namePart type="family">Lesch</namePart><namePart type="termsOfAddress">MD</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Claudia</namePart><namePart type="family">Sommer</namePart><namePart type="termsOfAddress">MD</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Jobst</namePart><namePart type="family">Meyer</namePart><namePart type="termsOfAddress">PhD</namePart><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="article" displayLabel="article"></genre><originInfo><publisher>Blackwell Science Inc</publisher><place><placeTerm type="text">350 Main Street , Malden , MA 02148 , USA</placeTerm></place><dateIssued encoding="w3cdtf">2005-02</dateIssued><edition>Accepted for publication May 19, 2004.</edition><copyrightDate encoding="w3cdtf">2005</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><internetMediaType>text/html</internetMediaType><extent unit="figures">1</extent><extent unit="references">26</extent></physicalDescription><abstract lang="en">Objective.—The present study is designed to further elucidate the molecular genetic basis of migraine with and without aura. Background.—Migraine is a common disease of as yet unknown etiology. Interest in ion channels in migraine has been spurred by molecular genetic findings in familial hemiplegic migraine, since familial hemiplegic migraine type 1 is caused by mutations in the calcium channel gene CACNA1A. Methods.—Given this role of ion channels in migraine, we assessed the potassium channel KCNN3 as a candidate gene for common migraine. We analyzed the highly polymorphic repeat region coding for a poly‐glutamine stretch, which constitutes part of the cytoplasmic tail of the channel protein. Results.—We found an excess of the allele coding for 15 poly‐glutamines in migraine patients. Conclusions.—The potassium channel KCNN3 may thus be of pathophysiological importance in migraine with and without aura.</abstract><subject lang="en"><genre>keywords</genre><topic>migraine</topic><topic>aura</topic><topic>potassium channel</topic><topic>KCNN3</topic><topic>poly‐glutamine</topic></subject><relatedItem type="host"><titleInfo><title>Headache: The Journal of Head and Face Pain</title></titleInfo><genre type="journal">journal</genre><identifier type="ISSN">0017-8748</identifier><identifier type="eISSN">1526-4610</identifier><identifier type="DOI">10.1111/(ISSN)1526-4610</identifier><identifier type="PublisherID">HEAD</identifier><part><date>2005</date><detail type="volume"><caption>vol.</caption><number>45</number></detail><detail type="issue"><caption>no.</caption><number>2</number></detail><extent unit="pages"><start>132</start><end>136</end><total>5</total></extent></part></relatedItem><identifier type="istex">A765B8E841FABF919A2522DCE0BC663DC69DAF33</identifier><identifier type="DOI">10.1111/j.1526-4610.2005.05027.x</identifier><identifier type="ArticleID">HEAD05027</identifier><recordInfo><recordContentSource>WILEY</recordContentSource><recordOrigin>Blackwell Science Inc</recordOrigin></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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