STUB1/CHIP mutations cause Gordon Holmes syndrome as part of a widespread multisystemic neurodegeneration: evidence from four novel mutations

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dc.contributor.author Bender, Benjamin
dc.contributor.author Reich, Selina
dc.contributor.author Synofzik, Matthis Benjamin
dc.contributor.author Hayer, Stefanie Nicole
dc.contributor.author Schöls, Ludger
dc.contributor.author Schüle-Freyer, Rebecca
dc.date.accessioned 2018-03-06T15:55:35Z
dc.date.available 2018-03-06T15:55:35Z
dc.date.issued 2017
dc.identifier.issn 1750-1172
dc.identifier.uri http://hdl.handle.net/10900/80999
dc.language.iso en de_DE
dc.publisher Biomed Central Ltd de_DE
dc.relation.uri http://dx.doi.org/10.1186/s13023-017-0580-x de_DE
dc.rights info:eu-repo/semantics/closedAccess
dc.subject.ddc 570 de_DE
dc.subject.ddc 610 de_DE
dc.title STUB1/CHIP mutations cause Gordon Holmes syndrome as part of a widespread multisystemic neurodegeneration: evidence from four novel mutations de_DE
dc.type Artikel de_DE
utue.quellen.id 20170815222223_01742
utue.personen.roh Hayer, Stefanie Nicole
utue.personen.roh Deconinck, Tine
utue.personen.roh Bender, Benjamin
utue.personen.roh Smets, Katrien
utue.personen.roh Zuechner, Stephan
utue.personen.roh Reich, Selina
utue.personen.roh Schoels, Ludger
utue.personen.roh Schuele, Rebecca
utue.personen.roh De Jonghe, Peter
utue.personen.roh Baets, Jonathan
utue.personen.roh Synofzik, Matthis
dcterms.isPartOf.ZSTitelID Orphanet Journal of Rare Diseases de_DE
dcterms.isPartOf.ZS-Issue Article 31 de_DE
dcterms.isPartOf.ZS-Volume 12 de_DE
utue.fakultaet 04 Medizinische Fakultät de_DE


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