Clinical phenotype in patients with α-synuclein Parkinson's disease living in Greece in comparison with patients with sporadic Parkinson's disease

OBJECTIVE—An Ala53Thr mutation of the α-synuclein gene has been recently identified as a rare cause of autosomal Parkinson's disease (PD). The clinical characteristics of 15 patients with PD living in Greece with the Ala53Thr α-synuclein mutation (α-synPD) were compared with patients with spora...

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Main Authors: Papapetropoulos, S, Paschalis, C, Athanassiadou, A, Papadimitriou, A, Ellul, J, Polymeropoulos, M, Papapetropoulos, T.
Formato: Artigo
Idioma:Inglês
Publicado: BMJ Group 2001
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Papers
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC1737360/
https://ncbi.nlm.nih.gov/pubmed/11309462
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jnnp.70.5.662
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