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Analysis of the α-synuclein G209A mutation in familial Parkinson's disease

✍ Scribed by Sepideh Zareparsi; Jeffrey Kay; Richard Camicioli; Patricia Kramer; John Nutt; Thomas Bird; Michael Litt; Haydeh Payami

Book ID
117296808
Publisher
The Lancet
Year
1998
Tongue
English
Weight
59 KB
Volume
351
Category
Article
ISSN
0140-6736

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## Abstract The motor and neuropsychological abnormalities in eight Greek patients with Parkinson's disease (PD) carrying the α‐synuclein gene mutation (G209A) were studied. These patients (five men, three women) belonged to six different families. Their symptoms started between 32–50 years of age