LRRK2 in Parkinson's disease: Genetic and clinical studies from patients
10.1111/j.1742-4658.2009.07344.x
Saved in:
Main Authors: | Kumari U., Tan E.K. |
---|---|
其他作者: | DUKE-NUS MEDICAL SCHOOL |
格式: | Article |
出版: |
Wiley
2018
|
主題: | |
在線閱讀: | http://scholarbank.nus.edu.sg/handle/10635/149143 |
標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|
機構: | National University of Singapore |
相似書籍
-
The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients
由: Tan E.K., et al.
出版: (2018) -
Genetic testing of LRRK2 in Parkinson's disease: Is there a clinical role?
由: Buhat D.M.L., et al.
出版: (2018) -
LRRK2 mutations are not frequent in Swiss patients with Parkinson's disease
由: Burgunder, J.-M., et al.
出版: (2011) -
Analysis of LRRK2 Gly2385Arg genetic variant in non-Chinese Asians
由: Tan E.-K., et al.
出版: (2018) -
Targeting LRRK2 in Parkinson's disease: an update on recent developments
由: Chan S.L., et al.
出版: (2018)