Loss-of-function mutations in the ATP13A2/PARK9 gene cause complicated hereditary spastic paraplegia (SPG78)

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dc.contributor.author Synofzik, Matthis Benjamin
dc.contributor.author Reichbauer, Jennifer
dc.contributor.author Schöls, Ludger
dc.contributor.author Schüle-Freyer, Rebecca
dc.date.accessioned 2018-03-06T14:06:32Z
dc.date.available 2018-03-06T14:06:32Z
dc.date.issued 2017
dc.identifier.issn 1460-2156
dc.identifier.uri http://hdl.handle.net/10900/80952
dc.language.iso en en
dc.publisher Oxford Univ Press de_DE
dc.relation.uri http://dx.doi.org/10.1093/brain/aww307 de_DE
dc.rights info:eu-repo/semantics/closedAccess
dc.subject.ddc 610 de_DE
dc.subject.ddc 570 de_DE
dc.title Loss-of-function mutations in the ATP13A2/PARK9 gene cause complicated hereditary spastic paraplegia (SPG78) de_DE
dc.type Artikel de_DE
utue.quellen.id 20170815222223_01879
utue.publikation.seiten 287-305 de_DE
utue.personen.roh Estrada-Cuzcano, Alejandro
utue.personen.roh Martin, Shaun
utue.personen.roh Chamova, Teodora
utue.personen.roh Synofzik, Matthis
utue.personen.roh Timmann, Dagmar
utue.personen.roh Holemans, Tine
utue.personen.roh Andreeva, Albena
utue.personen.roh Reichbauer, Jennifer
utue.personen.roh De Rycke, Riet
utue.personen.roh Chang, Dae-In
utue.personen.roh van Veen, Sarah
utue.personen.roh Samuel, Jean
utue.personen.roh Schoels, Ludger
utue.personen.roh Poppel, Thorsten
utue.personen.roh Sorensen, Danny Mollerup
utue.personen.roh Asselbergh, Bob
utue.personen.roh Klein, Christine
utue.personen.roh Zuchner, Stephan
utue.personen.roh Jordanova, Albena
utue.personen.roh Vangheluwe, Peter
utue.personen.roh Tournev, Ivailo
utue.personen.roh Schule, Rebecca
dcterms.isPartOf.ZSTitelID Brain de_DE
dcterms.isPartOf.ZS-Volume 140 de_DE
utue.fakultaet 04 Medizinische Fakultät de_DE


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