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Autor:
Shaun Z.S. Mok, Chee-Hoe Ng, Marc Fivaz, Valina L. Dawson, Xuezhi Ouyang, Ted M. Dawson, Fengwei Yu, Eng-King Tan, Kah-Leong Lim, Cherlyn Koh
Publikováno v:
The Journal of Neuroscience. 29:11257-11262
Mutations in theleucine-rich repeat kinase 2(LRRK2) gene are currently recognized as the most common genetic cause of parkinsonism. Among the large number of LRRK2 mutations identified to date, the G2019S variant is the most common. In Asia, however,