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Linking a genome‐wide association study signal to a LRRK2 coding variant in Parkinson's disease
Authors:Jia Nee Foo PhD  Sun Ju Chung MD  PhD  Louis C. Tan MD  Herty Liany MS  Ho‐Sung Ryu MD  Myunghee Hong MS  Tat Hung Koh MS  Ishak D. Irwan MS  Wing‐Lok Au MD  Kumar‐M. Prakash MD  Tin Aung MD  PhD  Ching‐Yu Cheng MD  PhD  Siow‐Ann Chong MD  Chiea Chuen Khor MD  PhD  Jimmy Lee MD  E‐Shyong Tai MD  PhD  Eranga N. Vithana PhD  Tien‐Yin Wong MD  PhD  Kyuyoung Song PhD  Eng‐King Tan MD
Affiliation:1. Human Genetics, Genome Institute of Singapore, A*STAR, Singapore;2. Department of Neurology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea;3. Department of Neurology, Singapore General Hospital, National Neuroscience Institute, Singapore;4. Department of Biochemistry and Molecular Biology, University of Ulsan College of Medicine, Seoul, Korea;5. Singapore Eye Research Institute, Singapore;6. Department of Ophthalmology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore;7. Duke‐National University of Singapore Graduate Medical School, Singapore;8. Institute of Mental Health, Singapore;9. Department of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore;10. Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, National University Health System, Singapore;11. Saw Swee Hock School of Public Health, National University of Singapore, National University Health System, Singapore
Abstract:
Keywords:Parkinson's disease  sequencing  genome‐wide association  human genetics  coding variants
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