Uniparental disomy determined by whole-exome sequencing in a spectrum of rare motoneuron diseases and ataxias

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dc.contributor.author Reichbauer, Jennifer
dc.contributor.author Schüle, Rebecca
dc.contributor.author Synofzik, Matthis Benjamin
dc.contributor.author Rattay, Tim Wilfried
dc.contributor.author Söhn, Anne
dc.contributor.author Schöls, Ludger
dc.date.accessioned 2019-06-03T14:35:08Z
dc.date.available 2019-06-03T14:35:08Z
dc.date.issued 2017
dc.identifier.issn 2324-9269
dc.identifier.uri http://hdl.handle.net/10900/89199
dc.language.iso en de_DE
dc.publisher Wiley de_DE
dc.relation.uri http://dx.doi.org/10.1002/mgg3.285 de_DE
dc.rights info:eu-repo/semantics/closedAccess
dc.subject.ddc 570 de_DE
dc.subject.ddc 610 de_DE
dc.title Uniparental disomy determined by whole-exome sequencing in a spectrum of rare motoneuron diseases and ataxias de_DE
dc.type Artikel de_DE
utue.quellen.id 20190131163842_02811
utue.publikation.seiten 280-286 de_DE
utue.personen.roh Bis, Dana M.
utue.personen.roh Schuele, Rebecca
utue.personen.roh Reichbauer, Jennifer
utue.personen.roh Synofzik, Matthis
utue.personen.roh Rattay, Tim W.
utue.personen.roh Soehn, Anne
utue.personen.roh de Jonghe, Peter
utue.personen.roh Schoels, Ludger
utue.personen.roh Zuchner, Stephan
dcterms.isPartOf.ZSTitelID Molecular Genetics & Genomic Medicine de_DE
dcterms.isPartOf.ZS-Issue 3 de_DE
dcterms.isPartOf.ZS-Volume 5 de_DE
utue.fakultaet 04 Medizinische Fakultät de_DE


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