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

Bis, Dana M.; Schuele, Rebecca; Reichbauer, Jennifer; Synofzik, Matthis; Rattay, Tim W.; Soehn, Anne; de Jonghe, Peter; Schoels, Ludger; Zuchner, Stephan

dc.contributor.author	Reichbauer, Jennifer
dc.contributor.author	Schüle-Freyer, Rebecca
dc.contributor.author	Synofzik, Matthis
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	Article	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