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

• 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.
• 其他作者: MEDICINE
• 格式: Article
• 出版: John Wiley and Sons Inc. 2018
• 主題: Coding variants; Genome-wide association; Human genetics; Parkinson's disease; Sequencing
• 在線閱讀: http://scholarbank.nus.edu.sg/handle/10635/150115
• 機構: National University of Singapore

10.1002/mds.26495