Infantile hypokinetic‐hypotonic syndrome due to two novel mutations of the tyrosine hydroxylase gene
Identifieur interne : 002487 ( Istex/Corpus ); précédent : 002486; suivant : 002488Infantile hypokinetic‐hypotonic syndrome due to two novel mutations of the tyrosine hydroxylase gene
Auteurs : Diane Doummar ; Fabienne Clot ; Marie Vidailhet ; Alexandra Afenjar ; Alexandra Durr ; Alexis Brice ; Cyril Mignot ; Agnès Guet ; Thierry Billette De Villemeur ; Diana RodriguezSource :
- Movement Disorders [ 0885-3185 ] ; 2009-04-30.
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DOI: 10.1002/mds.22455
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ISTEX:0019070C648EBE2495CE4F18BF3FE05C18F0388DLe document en format XML
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Paris, France</unparsedAffiliation></affiliation></affiliationGroup><fundingInfo><fundingAgency>French Dystonia Network</fundingAgency></fundingInfo><fundingInfo><fundingAgency>GIS Maladies Rares</fundingAgency></fundingInfo><supportingInformation><p> Additional Supporting Information may be found in the online version of this article. </p></supportingInformation></contentMeta></header></component></istex:document></istex:metadataXml><!--Version 0.6 générée le 4-12-2015--><mods version="3.6"><titleInfo lang="en"><title>Infantile hypokinetic‐hypotonic syndrome due to two novel mutations of the tyrosine hydroxylase gene</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Letters to the Editor</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Infantile hypokinetic‐hypotonic syndrome due to two novel mutations of the tyrosine hydroxylase gene</title></titleInfo><name type="personal"><namePart type="given">Diane</namePart><namePart type="family">Doummar</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>AP‐HP, Service de Neuropédiatrie, Hôpital Armand Trousseau, Paris, France</affiliation><description>Correspondence: AP‐HP, Service de Neuropédiatrie, Hôpital Armand Trousseau, Paris, France</description><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Fabienne</namePart><namePart type="family">Clot</namePart><namePart type="termsOfAddress">PhD</namePart><affiliation>AP‐HP, Département de Génétique et Cytogénétique, Hôpital Pitié Salpêtrière, Paris, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Marie</namePart><namePart type="family">Vidailhet</namePart><namePart type="termsOfAddress">MD, PhD</namePart><affiliation>AP‐HP, Département de Neurologie, Hôpital Pitié‐Salpêtrière, INSERM UMR_S679, Université Pierre et Marie Curie‐Paris 6, Paris, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Alexandra</namePart><namePart type="family">Afenjar</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>AP‐HP, Service de Neuropédiatrie, Hôpital Armand Trousseau, Paris, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Alexandra</namePart><namePart type="family">Durr</namePart><namePart type="termsOfAddress">MD, PhD</namePart><affiliation>AP‐HP, Département de Génétique et Cytogénétique, Hôpital Pitié Salpêtrière, INSERM UMR_S679, Université Pierre et Marie Curie‐Paris 6, Paris, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Alexis</namePart><namePart type="family">Brice</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>AP‐HP, Département de Génétique et Cytogénétique, Hôpital 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Disord.</title></titleInfo><note type="content"> Additional Supporting Information may be found in the online version of this article.</note><subject><genre>article category</genre><topic>Letter</topic></subject><identifier type="ISSN">0885-3185</identifier><identifier type="eISSN">1531-8257</identifier><identifier type="DOI">10.1002/(ISSN)1531-8257</identifier><identifier type="PublisherID">MDS</identifier><part><date>2009</date><detail type="volume"><caption>vol.</caption><number>24</number></detail><detail type="issue"><caption>no.</caption><number>6</number></detail><extent unit="pages"><start>943</start><end>945</end><total>3</total></extent></part></relatedItem><identifier type="istex">0019070C648EBE2495CE4F18BF3FE05C18F0388D</identifier><identifier type="DOI">10.1002/mds.22455</identifier><identifier type="ArticleID">MDS22455</identifier><accessCondition type="use and reproduction" contentType="copyright">Copyright © 2009 Movement Disorder Society</accessCondition><recordInfo><recordOrigin>Wiley Subscription Services, Inc., A Wiley Company</recordOrigin><recordContentSource>WILEY</recordContentSource></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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