Lack of Association of the UCHL-1 Gene with Parkinson's Disease in a Greek Cohort: A Haplotype-Tagging Approach

dc.creator	Xiromerisiou, G.	en
dc.creator	Kyratzi, E.	en
dc.creator	Dardiotis, E.	en
dc.creator	Bozi, M.	en
dc.creator	Tsimourtou, V.	en
dc.creator	Stamboulis, E.	en
dc.creator	Ralli, S.	en
dc.creator	Vassilatis, D.	en
dc.creator	Gourbali, V.	en
dc.creator	Kountra, P. M.	en
dc.creator	Fountas, K.	en
dc.creator	Papadimitriou, A.	en
dc.creator	Stefanis, L.	en
dc.creator	Hadjigeorgiou, G. M.	en
dc.date.accessioned	2015-11-23T10:54:20Z
dc.date.available	2015-11-23T10:54:20Z
dc.date.issued	2011
dc.identifier	10.1002/mds.23694
dc.identifier.issn	0885-3185
dc.identifier.uri	http://hdl.handle.net/11615/34713
dc.source	Movement Disorders	en
dc.source.uri	<Go to ISI>://WOS:000295024700033
dc.subject	SUSCEPTIBILITY GENE	en
dc.subject	S18Y	en
dc.subject	VARIANT	en
dc.subject	Clinical Neurology	en
dc.title	Lack of Association of the UCHL-1 Gene with Parkinson's Disease in a Greek Cohort: A Haplotype-Tagging Approach	en
dc.type	journalArticle	en

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