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

Kun-Rodrigues, Celia; Ganos, Christos; Guerreiro, Rita; Schneider, Susanne A.; Schulte, Claudia; Lesage, Suzanne; Darwent, Lee; Holmans, Peter; Singleton, Andrew; Bhatia, Kailash; Bras, Jose

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