A systematic screening to identify de novo mutations causing sporadic early-onset Parkinson's disease

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dc.contributor.author Schulte, Claudia
dc.date.accessioned 2016-06-17T13:03:54Z
dc.date.available 2016-06-17T13:03:54Z
dc.date.issued 2015
dc.identifier.issn 1460-2083
dc.identifier.uri http://hdl.handle.net/10900/70666
dc.language.iso en en
dc.publisher Oxford Univ Press de_DE
dc.relation.uri http://dx.doi.org/10.1093/hmg/ddv376
dc.rights info:eu-repo/semantics/closedAccess
dc.subject.ddc 570 de_DE
dc.subject.ddc 610 de_DE
dc.title A systematic screening to identify de novo mutations causing sporadic early-onset Parkinson's disease de_DE
dc.type Article de_DE
utue.quellen.id 20160427062602_00159
utue.publikation.seiten 6711-6720 de_DE
utue.personen.roh Kun-Rodrigues, Celia
utue.personen.roh Ganos, Christos
utue.personen.roh Guerreiro, Rita
utue.personen.roh Schneider, Susanne A.
utue.personen.roh Schulte, Claudia
utue.personen.roh Lesage, Suzanne
utue.personen.roh Darwent, Lee
utue.personen.roh Holmans, Peter
utue.personen.roh Singleton, Andrew
utue.personen.roh Bhatia, Kailash
utue.personen.roh Bras, Jose
dcterms.isPartOf.ZSTitelID Human Molecular Genetics de_DE
dcterms.isPartOf.ZS-Issue 23 de_DE
dcterms.isPartOf.ZS-Volume 24 de_DE
utue.fakultaet Sonstige
utue.fakultaet 04 Medizinische Fakultät


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