Mutated alpha-synuclein gene in two Greek kindreds with familial PD: Incomplete penetrance?

dc.creator	Papadimitriou, A.	en
dc.creator	Veletza, V.	en
dc.creator	Hadjigeorgiou, G. M.	en
dc.creator	Patrikiou, A.	en
dc.creator	Hirano, M.	en
dc.creator	Anastasopoulos, I.	en
dc.date.accessioned	2015-11-23T10:42:47Z
dc.date.available	2015-11-23T10:42:47Z
dc.date.issued	1999
dc.identifier.issn	0028-3878
dc.identifier.uri	http://hdl.handle.net/11615/31661
dc.description.abstract	The G209A mutation in the alpha-synuclein gene has been associated with autosomal dominant PD (ADPD) in a family from Contursi, Italy, and three apparently unrelated Greek families. Several groups around the world failed to identify the G209A mutation in a sizable series of familial and sporadic cases of PD. The authors present two additional Greek families with ADPD associated with the G209A mutation. In both families, asymptomatic carriers older than the expected age at onset were found.	en
dc.source	Neurology	en
dc.source.uri	<Go to ISI>://WOS:000078512900043
dc.subject	PARKINSONS-DISEASE	en
dc.subject	Clinical Neurology	en
dc.title	Mutated alpha-synuclein gene in two Greek kindreds with familial PD: Incomplete penetrance?	en
dc.type	journalArticle	en

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