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SNCA, LRRK2, MAPT polymorphisms and Parkinson's disease in Russia

✍ Scribed by Emelyanov, A.; Andoskin, P.; Yakimovskii, A.; Usenko, T.; Nuzhnyi, E.; Nikolaev, M.; Pchelina, S.

Book ID: 121357426
Publisher: Elsevier Science
Year: 2013
Tongue: English
Weight: 156 KB
Volume: 19
Category: Article
ISSN: 1353-8020
DOI: 10.1016/j.parkreldis.2013.06.003

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## Abstract Among mutations associated with autosomal dominant and sporadic Parkinson's disease (PD) the G2019S substitution in the leucine‐rich repeat kinase 2 (LRRK2) gene is the most frequently identified. To estimate its frequency in Russia, we analyzed 208 patients with PD from the Northwester