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

dc.creatorXiromerisiou, G.en
dc.creatorKyratzi, E.en
dc.creatorDardiotis, E.en
dc.creatorBozi, M.en
dc.creatorTsimourtou, V.en
dc.creatorStamboulis, E.en
dc.creatorRalli, S.en
dc.creatorVassilatis, D.en
dc.creatorGourbali, V.en
dc.creatorKountra, P. M.en
dc.creatorFountas, K.en
dc.creatorPapadimitriou, A.en
dc.creatorStefanis, L.en
dc.creatorHadjigeorgiou, G. M.en
dc.date.accessioned2015-11-23T10:54:20Z
dc.date.available2015-11-23T10:54:20Z
dc.date.issued2011
dc.identifier10.1002/mds.23694
dc.identifier.issn0885-3185
dc.identifier.urihttp://hdl.handle.net/11615/34713
dc.sourceMovement Disordersen
dc.source.uri<Go to ISI>://WOS:000295024700033
dc.subjectSUSCEPTIBILITY GENEen
dc.subjectS18Yen
dc.subjectVARIANTen
dc.subjectClinical Neurologyen
dc.titleLack of Association of the UCHL-1 Gene with Parkinson's Disease in a Greek Cohort: A Haplotype-Tagging Approachen
dc.typejournalArticleen


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