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

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

10.1016/j.neulet.2005.04.103

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Bibliographic Details
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.
Other Authors: DEPT OF PHARMACOLOGY
Format: Article
Published: Elsevier 2018
Subjects:
LRRK2
Mutation
Parkinson's disease
Online Access:http://scholarbank.nus.edu.sg/handle/10635/150233
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Institution: National University of Singapore

Internet

http://scholarbank.nus.edu.sg/handle/10635/150233

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