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Analysis of the α-synuclein gene dosage variation associated with autosomal dominant form of Parkinson’s disease

✍ Scribed by E. V. Semenova; M. I. Shadrina; P. A. Slominsky; S. N. Illarioshkin; G. Kh. Bagyeva; A. V. Karabanov; I. A. Ivanova-Smolenskaia; S. A. Limborska

Book ID: 110199747
Publisher: SP MAIK Nauka/Interperiodica
Year: 2009
Tongue: English
Weight: 172 KB
Volume: 45
Category: Article
ISSN: 1022-7954
DOI: 10.1134/s1022795409040176

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## Abstract Missense mutations of the α‐synuclein gene have been reported to explain a few kindreds with autosomal dominant Parkinson's disease (PD). In order to identify mutations in our PD patients, we have screened the coding region and 5′flanking region of the gene. DNA samples from 50 patients