THAP1 mutations are infrequent in spasmodic dysphonia
Identifieur interne : 001399 ( Istex/Corpus ); précédent : 001398; suivant : 001400THAP1 mutations are infrequent in spasmodic dysphonia
Auteurs : Justus Groen ; Eren Yildirim ; Katja Ritz ; Frank Baas ; Jacobus Van ; Freerk Van ; Ton Langeveld ; Marina TijssenSource :
- Movement Disorders [ 0885-3185 ] ; 2011-08-15.
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DOI: 10.1002/mds.23682
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Tijssen received research support from the Prinses Beatrix Fund.</p></note><note xml:id="fn2"><p>Full financial disclosures and author roles may be found in the online version of this article.</p></note><note xml:id="fn3"><p>This study was supported by the Prinses Beatrix Fund.</p></note></noteGroup></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>THAP1 mutations are infrequent in spasmodic dysphonia</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>mutations are infrequent in spasmodic dysphonia</title></titleInfo><name type="personal"><namePart type="given">Justus L.</namePart><namePart type="family">Groen</namePart><affiliation>Department of Neurology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands</affiliation><affiliation>Department of Neurogenetics, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Eren</namePart><namePart type="family">Yildirim</namePart><affiliation>Department of Neurology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Katja</namePart><namePart type="family">Ritz</namePart><affiliation>Department of Neurogenetics, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Frank</namePart><namePart type="family">Baas</namePart><affiliation>Department of Neurogenetics, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Jacobus J.</namePart><namePart type="family">van Hilten</namePart><affiliation>Department of Neurology, Leiden University Medical Centre, Leiden, The Netherlands</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Freerk W.</namePart><namePart type="family">van der Meulen</namePart><affiliation>Department of Otorhinolaryngology—Head and Neck Surgery, Academic Medical Center, University of Amsterdam, Amsterdam, the Netherlands</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Ton P.</namePart><namePart type="family">Langeveld</namePart><affiliation>Department of Otorhinolaryngology—Head and Neck Surgery, Leiden University Medical Center, Leiden, The Netherlands</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Marina A.J.</namePart><namePart type="family">Tijssen</namePart><affiliation>Department of Neurology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands</affiliation><description>Correspondence: Department of Neurology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands</description><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="review-article">letter</genre><originInfo><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><place><placeTerm type="text">Hoboken</placeTerm></place><dateIssued encoding="w3cdtf">2011-08-15</dateIssued><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="tables">1</extent><extent unit="references">7</extent><extent unit="words">1678</extent></physicalDescription><note type="content">*Relevant conflicts of interest/financial disclosures: Justus L Groen received an AMC Graduate School Scholarship. Katja Ritz and Marina A.J. Tijssen received research support from the Prinses Beatrix Fund.</note><note type="content">*Full financial disclosures and author roles may be found in the online version of this article.</note><note type="content">*This study was supported by the Prinses Beatrix Fund.</note><relatedItem type="host"><titleInfo><title>Movement Disorders</title></titleInfo><titleInfo type="abbreviated"><title>Mov. Disord.</title></titleInfo><subject><genre>article category</genre><topic>Letters: New Observation</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>2011</date><detail type="volume"><caption>vol.</caption><number>26</number></detail><detail type="issue"><caption>no.</caption><number>10</number></detail><extent unit="pages"><start>1952</start><end>1954</end><total>3</total></extent></part></relatedItem><identifier type="istex">38C07C1F91CD35D74E20344A57905312EC9F9F2A</identifier><identifier type="DOI">10.1002/mds.23682</identifier><identifier type="ArticleID">MDS23682</identifier><accessCondition type="use and reproduction" contentType="copyright">Copyright © 2011 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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