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Worldwide frequency of G2019S LRRK2 mutation in Parkinson's disease: A systematic review

✍ Scribed by L. Correia Guedes; J.J. Ferreira; M.M. Rosa; M. Coelho; V. Bonifati; C. Sampaio

Book ID
116820728
Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
408 KB
Volume
16
Category
Article
ISSN
1353-8020

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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