No evidence for THAP1/DYT6 variants as disease modifiers in DYT1 dystonia
Identifieur interne : 002475 ( Istex/Corpus ); précédent : 002474; suivant : 002476No evidence for THAP1/DYT6 variants as disease modifiers in DYT1 dystonia
Auteurs : Christoph Kamm ; Nils Uflacker ; Friedrich Asmus ; Christoph Schrader ; Alexander Wolters ; Matthias Wittstock ; Jens Pahnke ; Thomas Gasser ; Jens Volkmann ; Alexander Münchau ; Johann Hagenah ; Reiner Benecke ; Christine Klein ; Katja LohmannSource :
- Movement Disorders [ 0885-3185 ] ; 2011-09.
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DOI: 10.1002/mds.23777
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Christoph" sort="Kamm, Christoph" uniqKey="Kamm C" first="Christoph" last="Kamm">Christoph Kamm</name><affiliation><mods:affiliation>Department of Neurology, University of Rostock, Rostock, Germany</mods:affiliation></affiliation></author><author><name sortKey="Uflacker, Nils" sort="Uflacker, Nils" uniqKey="Uflacker N" first="Nils" last="Uflacker">Nils Uflacker</name><affiliation><mods:affiliation>Section of Clinical and Molecular Neurogenetics at the Department of Neurology University of Lubeck, Lubeck, Germany</mods:affiliation></affiliation></author><author><name sortKey="Asmus, Friedrich" sort="Asmus, Friedrich" uniqKey="Asmus F" first="Friedrich" last="Asmus">Friedrich Asmus</name><affiliation><mods:affiliation>Department of Neurodegenerative Diseases, Hertie‐Institute for Clinical Brain Research, University of Tubingen, Tubingen, Germany</mods:affiliation></affiliation></author><author><name sortKey="Schrader, Christoph" sort="Schrader, Christoph" uniqKey="Schrader C" first="Christoph" last="Schrader">Christoph Schrader</name><affiliation><mods:affiliation>Department of Neurology, Hannover Medical School, Hannover, Germany</mods:affiliation></affiliation></author><author><name sortKey="Wolters, Alexander" sort="Wolters, Alexander" uniqKey="Wolters A" first="Alexander" last="Wolters">Alexander Wolters</name><affiliation><mods:affiliation>Department of Neurology, University of Rostock, Rostock, Germany</mods:affiliation></affiliation></author><author><name sortKey="Wittstock, Matthias" sort="Wittstock, Matthias" uniqKey="Wittstock M" first="Matthias" last="Wittstock">Matthias Wittstock</name><affiliation><mods:affiliation>Department of Neurology, University of Rostock, Rostock, Germany</mods:affiliation></affiliation></author><author><name sortKey="Pahnke, Jens" sort="Pahnke, Jens" uniqKey="Pahnke J" first="Jens" last="Pahnke">Jens Pahnke</name><affiliation><mods:affiliation>Department of Neurology, University of Rostock, Rostock, 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dystonia</title><publicationDate>2011</publicationDate><copyrightDate>2011</copyrightDate><doi><json:string>10.1002/mds.23777</json:string></doi><id>797115C44FBFAD66D39E7F389967E2EEA97EDCFE</id><fulltext><json:item><original>true</original><mimetype>application/pdf</mimetype><extension>pdf</extension><uri>https://api.istex.fr/document/797115C44FBFAD66D39E7F389967E2EEA97EDCFE/fulltext/pdf</uri></json:item><json:item><original>false</original><mimetype>application/zip</mimetype><extension>zip</extension><uri>https://api.istex.fr/document/797115C44FBFAD66D39E7F389967E2EEA97EDCFE/fulltext/zip</uri></json:item><istex:fulltextTEI uri="https://api.istex.fr/document/797115C44FBFAD66D39E7F389967E2EEA97EDCFE/fulltext/tei"><teiHeader type="text"><fileDesc><titleStmt><title level="a" type="main" xml:lang="en">No evidence for THAP1/DYT6 variants as disease modifiers in DYT1 dystonia</title></titleStmt><publicationStmt><authority>ISTEX</authority><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>Hoboken</pubPlace><availability><p>Wiley Subscription Services, Inc., A Wiley Company</p></availability><date>2011</date></publicationStmt><notesStmt><note type="content">*Funding agencies: This work was supported in part by the Genetic Network for Hereditary Movement Disorders (GeNeMove, 01GM0304, http://www.genemove.org), funded by the German Ministry for Education and Research (GMER, BMBF), and by research grants from the German Research Foundation (LO1555/3‐1 to Katja Lohmann), the Hermann and Lilly Schilling Foundation, and the Volkswagen Foundation (to Christine Klein).</note><note type="content">*Relevant conflicts of interest/financial disclosures: Nothing to report.</note><note type="content">*Full financial disclosures and author roles may be found in the online version of this article.</note></notesStmt><sourceDesc><biblStruct type="inbook"><analytic><title level="a" type="main" xml:lang="en">No evidence for THAP1/DYT6 variants as disease modifiers in DYT1 dystonia</title><author><persName><forename type="first">Christoph</forename><surname>Kamm</surname><roleName type="degree">MD</roleName></persName><note type="correspondence"><p>Correspondence: Department of Neurology, University of Rostock, Rostock, Germany</p></note><affiliation>Department of Neurology, University of Rostock, Rostock, Germany</affiliation></author><author><persName><forename type="first">Nils</forename><surname>Uflacker</surname></persName><affiliation>Section of Clinical and Molecular Neurogenetics at the Department of Neurology University of Lubeck, Lubeck, Germany</affiliation></author><author><persName><forename type="first">Friedrich</forename><surname>Asmus</surname><roleName type="degree">MD</roleName></persName><affiliation>Department of Neurodegenerative Diseases, Hertie‐Institute for Clinical Brain Research, University of Tubingen, Tubingen, Germany</affiliation></author><author><persName><forename type="first">Christoph</forename><surname>Schrader</surname></persName><affiliation>Department of Neurology, Hannover Medical School, Hannover, Germany</affiliation></author><author><persName><forename type="first">Alexander</forename><surname>Wolters</surname></persName><affiliation>Department of Neurology, University of Rostock, Rostock, Germany</affiliation></author><author><persName><forename type="first">Matthias</forename><surname>Wittstock</surname></persName><affiliation>Department of Neurology, University of Rostock, Rostock, Germany</affiliation></author><author><persName><forename type="first">Jens</forename><surname>Pahnke</surname></persName><affiliation>Department of Neurology, University of Rostock, Rostock, Germany</affiliation></author><author><persName><forename type="first">Thomas</forename><surname>Gasser</surname><roleName type="degree">MD</roleName></persName><affiliation>Department of Neurodegenerative Diseases, Hertie‐Institute for Clinical Brain Research, 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number="0"></count><count type="tableTotal" number="0"></count><count type="referenceTotal" number="7"></count><count type="wordTotal" number="2008"></count></countGroup><titleGroup><title type="main" xml:lang="en">No evidence for <i>THAP1</i>/<i>DYT6</i> variants as disease modifiers in DYT1 dystonia<link href="#fn1"></link><link href="#fn2"></link><link href="#fn3"></link></title><title type="short" xml:lang="en">Letters to the Editors</title></titleGroup><creators><creator xml:id="au1" creatorRole="author" affiliationRef="#af1" corresponding="yes"><personName><givenNames>Christoph</givenNames><familyName>Kamm</familyName><degrees>MD</degrees></personName><contactDetails><email normalForm="christoph.kamm@med.uni-rostock.de">christoph.kamm@med.uni‐rostock.de</email></contactDetails></creator><creator xml:id="au2" creatorRole="author" affiliationRef="#af2"><personName><givenNames>Nils</givenNames><familyName>Uflacker</familyName></personName></creator><creator xml:id="au3" 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affiliationRef="#af3"><personName><givenNames>Thomas</givenNames><familyName>Gasser</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au9" creatorRole="author" affiliationRef="#af5"><personName><givenNames>Jens</givenNames><familyName>Volkmann</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au10" creatorRole="author" affiliationRef="#af6"><personName><givenNames>Alexander</givenNames><familyName>Münchau</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au11" creatorRole="author" affiliationRef="#af2"><personName><givenNames>Johann</givenNames><familyName>Hagenah</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au12" creatorRole="author" affiliationRef="#af1"><personName><givenNames>Reiner</givenNames><familyName>Benecke</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au13" creatorRole="author" affiliationRef="#af2"><personName><givenNames>Christine</givenNames><familyName>Klein</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au14" creatorRole="author" affiliationRef="#af2"><personName><givenNames>Katja</givenNames><familyName>Lohmann</familyName><degrees>PhD</degrees></personName></creator></creators><affiliationGroup><affiliation xml:id="af1" countryCode="DE" type="organization"><unparsedAffiliation>Department of Neurology, University of Rostock, Rostock, Germany</unparsedAffiliation></affiliation><affiliation xml:id="af2" countryCode="DE" type="organization"><unparsedAffiliation>Section of Clinical and Molecular Neurogenetics at the Department of Neurology University of Lubeck, Lubeck, Germany</unparsedAffiliation></affiliation><affiliation xml:id="af3" countryCode="DE" type="organization"><unparsedAffiliation>Department of Neurodegenerative Diseases, Hertie‐Institute for Clinical Brain Research, University of Tubingen, Tubingen, Germany</unparsedAffiliation></affiliation><affiliation xml:id="af4" countryCode="DE" type="organization"><unparsedAffiliation>Department of Neurology, Hannover Medical School, Hannover, Germany</unparsedAffiliation></affiliation><affiliation xml:id="af5" countryCode="DE" type="organization"><unparsedAffiliation>Department of Neurology, Christian‐Albrechts‐University, Kiel, Germany</unparsedAffiliation></affiliation><affiliation xml:id="af6" countryCode="DE" type="organization"><unparsedAffiliation>Department of Neurology, University Medical Center Hamburg Eppendorf, Hamburg, Germany</unparsedAffiliation></affiliation><affiliation xml:id="af7" countryCode="DE" type="organization"><unparsedAffiliation>Department of Neurology, University of Rostock, Rostock, Germany</unparsedAffiliation></affiliation><affiliation xml:id="af8" countryCode="DE" type="organization"><unparsedAffiliation>Section of Clinical and Molecular Neurogenetics at the Department of Neurology, University of Lubeck, Lubeck, Germany</unparsedAffiliation></affiliation><affiliation xml:id="af9" countryCode="DE" type="organization"><unparsedAffiliation>Department of Neurodegenerative Diseases, Hertie‐Institute for Clinical Brain Research, University of Tubingen, Tubingen, Germany</unparsedAffiliation></affiliation><affiliation xml:id="af10" countryCode="DE" type="organization"><unparsedAffiliation>Department of Neurology, Hannover Medical School, Hannover, Germany</unparsedAffiliation></affiliation><affiliation xml:id="af11" countryCode="DE" type="organization"><unparsedAffiliation>Department of Neurology, Christian‐Albrechts‐University, Kiel, Germany</unparsedAffiliation></affiliation><affiliation xml:id="af12" countryCode="DE" type="organization"><unparsedAffiliation>Department of Neurology, University Medical Center Hamburg‐Eppendorf, Hamburg, Germany</unparsedAffiliation></affiliation></affiliationGroup></contentMeta><noteGroup><note xml:id="fn1"><p><b>Funding agencies:</b> This work was supported in part by the <span cssStyle="text-decoration:underline">Ge</span>netic <span cssStyle="text-decoration:underline">Ne</span>twork for Hereditary <span cssStyle="text-decoration:underline">Move</span>ment Disorders (GeNeMove, 01GM0304, <url href="http://www.genemove.org">http://www.genemove.org</url>), funded by the German Ministry for Education and Research (GMER, BMBF), and by research grants from the German Research Foundation (LO1555/3‐1 to Katja Lohmann), the Hermann and Lilly Schilling Foundation, and the Volkswagen Foundation (to Christine Klein).</p></note><note xml:id="fn2"><p><b>Relevant conflicts of interest/financial disclosures:</b> Nothing to report.</p></note><note xml:id="fn3"><p>Full financial disclosures and author roles may be found in the online version of this article.</p></note></noteGroup></header></component></istex:document></istex:metadataXml><!--Version 0.6 générée le 3-12-2015--><mods version="3.6"><titleInfo lang="en"><title>No evidence for THAP1/DYT6 variants as disease modifiers in DYT1 dystonia</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Letters to the Editors</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>No evidence for</title></titleInfo><name type="personal"><namePart type="given">Christoph</namePart><namePart type="family">Kamm</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Neurology, University of Rostock, Rostock, Germany</affiliation><description>Correspondence: Department of Neurology, University of Rostock, Rostock, Germany</description><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Nils</namePart><namePart type="family">Uflacker</namePart><affiliation>Section of Clinical and Molecular Neurogenetics at the Department of Neurology University of Lubeck, Lubeck, Germany</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Friedrich</namePart><namePart type="family">Asmus</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Neurodegenerative Diseases, Hertie‐Institute for Clinical Brain Research, University of Tubingen, Tubingen, Germany</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Christoph</namePart><namePart type="family">Schrader</namePart><affiliation>Department of Neurology, Hannover Medical School, Hannover, Germany</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Alexander</namePart><namePart type="family">Wolters</namePart><affiliation>Department of Neurology, University of Rostock, Rostock, Germany</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Matthias</namePart><namePart type="family">Wittstock</namePart><affiliation>Department of Neurology, University of Rostock, Rostock, Germany</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Jens</namePart><namePart type="family">Pahnke</namePart><affiliation>Department of Neurology, University of Rostock, Rostock, Germany</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Thomas</namePart><namePart type="family">Gasser</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Neurodegenerative Diseases, Hertie‐Institute for Clinical Brain Research, University of Tubingen, Tubingen, Germany</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Jens</namePart><namePart type="family">Volkmann</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Neurology, Christian‐Albrechts‐University, Kiel, Germany</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Alexander</namePart><namePart type="family">Münchau</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Neurology, University Medical Center Hamburg Eppendorf, Hamburg, Germany</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Johann</namePart><namePart type="family">Hagenah</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Section of Clinical and Molecular Neurogenetics at the Department of Neurology University of Lubeck, Lubeck, Germany</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Reiner</namePart><namePart type="family">Benecke</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Neurology, University of Rostock, Rostock, Germany</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Christine</namePart><namePart type="family">Klein</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Section of Clinical and Molecular Neurogenetics at the Department of Neurology University of Lubeck, Lubeck, Germany</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Katja</namePart><namePart type="family">Lohmann</namePart><namePart type="termsOfAddress">PhD</namePart><affiliation>Section of Clinical and Molecular Neurogenetics at the Department of Neurology University of Lubeck, Lubeck, Germany</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre authority="originalCategForm">letter</genre><originInfo><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><place><placeTerm type="text">Hoboken</placeTerm></place><dateIssued encoding="w3cdtf">2011-09</dateIssued><dateCaptured encoding="w3cdtf">2011-01-21</dateCaptured><dateValid encoding="w3cdtf">2011-04-08</dateValid><copyrightDate encoding="w3cdtf">2011</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="references">7</extent><extent unit="words">2008</extent></physicalDescription><note type="content">*Funding agencies: This work was supported in part by the Genetic Network for Hereditary Movement Disorders (GeNeMove, 01GM0304, http://www.genemove.org), funded by the German Ministry for Education and Research (GMER, BMBF), and by research grants from the German Research Foundation (LO1555/3‐1 to Katja Lohmann), the Hermann and Lilly Schilling Foundation, and the Volkswagen Foundation (to Christine Klein).</note><note type="content">*Relevant conflicts of interest/financial disclosures: Nothing to report.</note><note type="content">*Full financial disclosures and author roles may be found in the online version of this article.</note><relatedItem type="host"><titleInfo><title>Movement Disorders</title></titleInfo><titleInfo type="abbreviated"><title>Mov. 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