Uniparental disomy of chromosome 16 unmasks recessive mutations of FA2H/SPG35 in 4 families

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dc.contributor.author Söhn, Anne
dc.contributor.author Rattay, Tim Wilfried
dc.contributor.author Beck-Wödl, Stefanie
dc.contributor.author Schäferhoff, Karin
dc.contributor.author Döbler-Neumann, Marion
dc.contributor.author Rieß, Olaf
dc.contributor.author Schüle-Freyer, Rebecca
dc.contributor.author Bauer, Peter
dc.contributor.author Schöls, Ludger
dc.date.accessioned 2019-03-01T13:21:37Z
dc.date.available 2019-03-01T13:21:37Z
dc.date.issued 2016
dc.identifier.issn 1526-632X
dc.identifier.uri http://hdl.handle.net/10900/86580
dc.language.iso en de_DE
dc.publisher Lippincott Williams & Wilkins de_DE
dc.relation.uri http://dx.doi.org/10.1212/WNL.0000000000002843 de_DE
dc.rights info:eu-repo/semantics/closedAccess
dc.subject.ddc 610 de_DE
dc.title Uniparental disomy of chromosome 16 unmasks recessive mutations of FA2H/SPG35 in 4 families de_DE
dc.type Artikel de_DE
utue.quellen.id 20180405102126_02002
utue.publikation.seiten 186-191 de_DE
utue.personen.roh Soehn, Anne S.
utue.personen.roh Rattay, Tim W.
utue.personen.roh Beck-Woedl, Stefanie
utue.personen.roh Schaeferhoff, Karin
utue.personen.roh Monk, David
utue.personen.roh Doebler-Neumann, Marion
utue.personen.roh Hoertnagel, Konstanze
utue.personen.roh Schluter, Agatha
utue.personen.roh Ruiz, Montserrat
utue.personen.roh Pujol, Aurora
utue.personen.roh Zuchner, Stephan
utue.personen.roh Riess, Olaf
utue.personen.roh Schule, Rebecca
utue.personen.roh Bauer, Peter
utue.personen.roh Schoels, Ludger
dcterms.isPartOf.ZSTitelID Neurology de_DE
dcterms.isPartOf.ZS-Issue 2 de_DE
dcterms.isPartOf.ZS-Volume 87 de_DE
utue.fakultaet 04 Medizinische Fakultät de_DE


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