Linking a genome-wide association study signal to a LRRK2 coding variant in Parkinson's disease

Linking a genome-wide association study signal to a LRRK2 coding variant in Parkinson's disease

10.1002/mds.26495

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Bibliographic Details
Main Authors:	Foo J.N., Chung S.J., Tan L.C., Liany H., Ryu H.-S., Hong M., Koh T.H., Irwan I.D., Au W.-L., Prakash K.-M., Aung T., Cheng C.-Y., Chong S.-A., Khor C.C., Lee J., Tai E.-S., Vithana E.N., Wong T.-Y., Song K., Liu J., Tan E.-K.
Other Authors:	DUKE-NUS MEDICAL SCHOOL
Format:	Article
Published:	John Wiley and Sons Inc. 2018
Subjects:	Coding variants Genome-wide association Human genetics Parkinson's disease Sequencing
Online Access:	http://scholarbank.nus.edu.sg/handle/10635/150115
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Institution:	National University of Singapore

Description
Summary:	10.1002/mds.26495