Mutations in phospholipase DDHD2 cause autosomal recessive hereditary spastic paraplegia (SPG54)

Gonzalez, Michael; Nampoothiri, Sheela; Kornblum, Cornelia; Oteyza, Andres Caballero; Walter, Jochen; Konidari, Ioanna; Hulme, William; Speziani, Fiorella; Schoels, Ludger; Zuechner, Stephan; Schuele, Rebecca

dc.contributor.author	Schöls, Ludger
dc.contributor.author	Schüle-Freyer, Rebecca
dc.contributor.author	Caballero Oteyza, Andrés
dc.date.accessioned	2014-02-04T07:53:00Z
dc.date.available	2014-02-04T07:53:00Z
dc.date.issued	2013
dc.identifier.issn	1018-4813
dc.identifier.uri	http://hdl.handle.net/10900/40475
dc.language.iso	en	en
dc.publisher	Nature Publishing Group	de_DE
dc.relation.uri	http://dx.doi.org/10.1038/ejhg.2013.29	de_DE
dc.rights	info:eu-repo/semantics/closedAccess
dc.subject.ddc	570	de_DE
dc.subject.ddc	610	de_DE
dc.title	Mutations in phospholipase DDHD2 cause autosomal recessive hereditary spastic paraplegia (SPG54)	de_DE
dc.type	Article	de_DE
utue.quellen.id	20140116051827_00338	de_DE
utue.publikation.seiten	1214-1218	de_DE
utue.personen.roh	Gonzalez, Michael
utue.personen.roh	Nampoothiri, Sheela
utue.personen.roh	Kornblum, Cornelia
utue.personen.roh	Oteyza, Andres Caballero
utue.personen.roh	Walter, Jochen
utue.personen.roh	Konidari, Ioanna
utue.personen.roh	Hulme, William
utue.personen.roh	Speziani, Fiorella
utue.personen.roh	Schoels, Ludger
utue.personen.roh	Zuechner, Stephan
utue.personen.roh	Schuele, Rebecca
dcterms.isPartOf.ZSTitelID	European Journal of Human Genetics	de_DE
dcterms.isPartOf.ZS-Issue	11	de_DE
dcterms.isPartOf.ZS-Volume	21	de_DE
utue.fakultaet	04 Medizinische Fakultät	de_DE