Phenotype and frequency of STUB1 mutations: next-generation screenings in Caucasian ataxia and spastic paraplegia cohorts

Synofzik, Matthis; Schuele, Rebecca; Schulze, Martin; Gburek-Augustat, Janina; Schweizer, Roland; Schirmacher, Anja; Kraegeloh-Mann, Ingeborg; Gonzalez, Michael; Young, Peter; Zuechner, Stephan; Schoels, Ludger; Bauer, Peter

dc.contributor.author	Schulze, Martin
dc.contributor.author	Gburek-Augustat, Janina
dc.contributor.author	Schweizer, Roland
dc.contributor.author	Bauer, Peter
dc.contributor.author	Synofzik, Matthis
dc.contributor.author	Schüle-Freyer, Rebecca
dc.contributor.author	Krägeloh-Mann, Ingeborg
dc.contributor.author	Schöls, Ludger
dc.date.accessioned	2014-08-06T09:01:48Z
dc.date.available	2014-08-06T09:01:48Z
dc.date.issued	2014
dc.identifier.issn	1750-1172
dc.identifier.uri	http://hdl.handle.net/10900/55250
dc.language.iso	en	en
dc.publisher	Biomed Central Ltd	de_DE
dc.relation.uri	http://dx.doi.org/10.1186/1750-1172-9-57	de_DE
dc.rights	info:eu-repo/semantics/closedAccess
dc.subject.ddc	570	de_DE
dc.subject.ddc	610	de_DE
dc.title	Phenotype and frequency of STUB1 mutations: next-generation screenings in Caucasian ataxia and spastic paraplegia cohorts	de_DE
dc.type	Article	de_DE
utue.quellen.id	20140610213910_00144	de_DE
utue.personen.roh	Synofzik, Matthis
utue.personen.roh	Schuele, Rebecca
utue.personen.roh	Schulze, Martin
utue.personen.roh	Gburek-Augustat, Janina
utue.personen.roh	Schweizer, Roland
utue.personen.roh	Schirmacher, Anja
utue.personen.roh	Kraegeloh-Mann, Ingeborg
utue.personen.roh	Gonzalez, Michael
utue.personen.roh	Young, Peter
utue.personen.roh	Zuechner, Stephan
utue.personen.roh	Schoels, Ludger
utue.personen.roh	Bauer, Peter
dcterms.isPartOf.ZSTitelID	Orphanet Journal of Rare Diseases	de_DE
dcterms.isPartOf.ZS-Issue	Article 57	de_DE
dcterms.isPartOf.ZS-Volume	9	de_DE
utue.fakultaet	04 Medizinische Fakultät	de_DE