Identification of a de novo mutation in SPG11
Identifieur interne : 002763 ( Istex/Corpus ); précédent : 002762; suivant : 002764Identification of a de novo mutation in SPG11
Auteurs : Paola S. Denora ; Knut Brockmann ; Marianna Ciccolella ; Jeremy Truchetto ; Giovanni Stevanin ; Filippo M. SantorelliSource :
- Movement Disorders [ 0885-3185 ] ; 2010-03-15.
Url:
DOI: 10.1002/mds.22964
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ISTEX:5F0B26E472132EF4678DA8A294B26A0A54B58DF4Le document en format XML
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type="personal"><namePart type="given">Paola S.</namePart><namePart type="family">Denora</namePart><namePart type="termsOfAddress">PhD</namePart><affiliation>INSERM, UMR_S975 (formerly U679), Paris, France</affiliation><affiliation>UPMC University Paris 06, UMR_S975, Centre de Recherche Institut du cerveau et de la Moelle Epiniere, CNRS 7225, Paris, France</affiliation><affiliation>Unit of Molecular Medicine, IRCCS‐Bambino Gesu' Children's Hospital, Rome, Italy</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Knut</namePart><namePart type="family">Brockmann</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Pediatrics and Neuropediatrics, University of Gottingen, Germany</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Marianna</namePart><namePart type="family">Ciccolella</namePart><namePart type="termsOfAddress">BS</namePart><affiliation>Unit of Molecular Medicine, IRCCS‐Bambino Gesu' Children's Hospital, Rome, Italy</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Jeremy</namePart><namePart type="family">Truchetto</namePart><namePart type="termsOfAddress">MS</namePart><affiliation>INSERM, UMR_S975 (formerly U679), Paris, France</affiliation><affiliation>UPMC University Paris 06, UMR_S975, Centre de Recherche Institut du cerveau et de la Moelle Epiniere, CNRS 7225, Paris, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Giovanni</namePart><namePart type="family">Stevanin</namePart><namePart type="termsOfAddress">PhD</namePart><affiliation>INSERM, UMR_S975 (formerly U679), Paris, France</affiliation><affiliation>UPMC University Paris 06, UMR_S975, Centre de Recherche Institut du cerveau et de la Moelle Epiniere, CNRS 7225, Paris, France</affiliation><affiliation>APHP, Departement de Genetique et Cytogenetique, Groupe Hospitalier Universitaire Pitie‐Salpetriere, Paris, France</affiliation><affiliation>Giovanni Stevanin, INSERM, UMR_S975 (formerly U679), Paris, FranceFilippo M. Santorelli, Unit of Molecular Medicine, IRCCS‐Bambino Gesu' Children's Hospital, Rome, Italy</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Filippo M.</namePart><namePart type="family">Santorelli</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Unit of Molecular Medicine, IRCCS‐Bambino Gesu' Children's Hospital, Rome, Italy</affiliation><affiliation>Giovanni Stevanin, INSERM, UMR_S975 (formerly U679), Paris, FranceFilippo M. Santorelli, Unit of Molecular Medicine, IRCCS‐Bambino Gesu' Children's Hospital, Rome, Italy</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">2010-03-15</dateIssued><copyrightDate encoding="w3cdtf">2010</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="tables">1</extent><extent unit="references">8</extent><extent unit="words">1516</extent></physicalDescription><note type="funding">Italian Ministry of Health</note><note type="funding">E‐RARE grant from the European Union (EUROSPA network)</note><relatedItem type="host"><titleInfo><title>Movement Disorders</title></titleInfo><titleInfo type="abbreviated"><title>Mov. Disord.</title></titleInfo><subject><genre>article category</genre><topic>Letter to the Editor</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>2010</date><detail type="volume"><caption>vol.</caption><number>25</number></detail><detail type="issue"><caption>no.</caption><number>4</number></detail><extent unit="pages"><start>501</start><end>503</end><total>2</total></extent></part></relatedItem><identifier type="istex">5F0B26E472132EF4678DA8A294B26A0A54B58DF4</identifier><identifier type="DOI">10.1002/mds.22964</identifier><identifier type="ArticleID">MDS22964</identifier><accessCondition type="use and reproduction" contentType="copyright">Copyright © 2010 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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