The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients

• Main Authors: Tan E.K., Shen H., Tan L.C.S., Farrer M., Yew K., Chua E., Jamora R.D., Puvan K., Puong K.Y., Zhao Y., Pavanni R., Wong M.C., Yih Y., Skipper L., Liu J.-J.
• 其他作者: PHARMACOLOGY
• 格式: Article
• 出版: Elsevier 2018
• 主題: LRRK2; Mutation; Parkinson's disease
• 在線閱讀: http://scholarbank.nus.edu.sg/handle/10635/150233

10.1016/j.neulet.2005.04.103