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

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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 Benjamin
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 Artikel 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


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