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Screening for SNCA and LRRK2 mutations in Greek sporadic and autosomal dominant PD: identification of two novel LRRK2 variants

dc.creatorYiromerisiou, G.en
dc.creatorGourbali, V.en
dc.creatorDardiotis, E.en
dc.creatorDardioti, M.en
dc.creatorTsimourtou, V.en
dc.creatorAggelakis, K.en
dc.creatorPapakonstaninou, I.en
dc.creatorNoulas, G.en
dc.creatorPapadimitriou, A.en
dc.creatorSingleton, A.en
dc.creatorHadjigeorgiou, G.en
dc.date.accessioned2015-11-23T10:54:27Z
dc.date.available2015-11-23T10:54:27Z
dc.date.issued2006
dc.identifier.issn0340-5354
dc.identifier.urihttp://hdl.handle.net/11615/34742
dc.source.uri<Go to ISI>://WOS:000238478600129
dc.subjectClinical Neurologyen
dc.titleScreening for SNCA and LRRK2 mutations in Greek sporadic and autosomal dominant PD: identification of two novel LRRK2 variantsen
dc.typejournalArticleen


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