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

Hayer, Stefanie Nicole; Deconinck, Tine; Bender, Benjamin; Smets, Katrien; Zuechner, Stephan; Reich, Selina; Schoels, Ludger; Schuele, Rebecca; De Jonghe, Peter; Baets, Jonathan; Synofzik, Matthis

dc.contributor.author	Bender, Benjamin
dc.contributor.author	Reich, Selina
dc.contributor.author	Synofzik, Matthis
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	Article	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