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Lack of mutation G209A in the alpha-synuclein gene in French patients with familial and sporadic Parkinson's disease



Lack of mutation G209A in the alpha-synuclein gene in French patients with familial and sporadic Parkinson's disease



Journal of Neurology, Neurosurgery, and Psychiatry 65(6): 948-949




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Accession: 010907069

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PMID: 9854985


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