Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease
10.1093/hmg/ddi376
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Oxford University Press
2018
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| Online Access: | http://scholarbank.nus.edu.sg/handle/10635/150224 |
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sg-nus-scholar.10635-1502242024-11-09T18:18:53Z Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease Skipper L. Li Y. Bonnard C. Pavanni R. Yih Y. Chua E. Sung W.-K. Tan L. Wong M.-C. Tan E.-K. Liu J. DEPARTMENT OF COMPUTER SCIENCE GENOME INSTITUTE OF SINGAPORE DUKE-NUS MEDICAL SCHOOL 10.1093/hmg/ddi376 Human Molecular Genetics 14 23 3549-3556 2018-12-27T03:19:40Z 2018-12-27T03:19:40Z 2005 Article Skipper L., Li Y., Bonnard C., Pavanni R., Yih Y., Chua E., Sung W.-K., Tan L., Wong M.-C., Tan E.-K., Liu J. (2005). Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease. Human Molecular Genetics 14 (23) : 3549-3556. ScholarBank@NUS Repository. https://doi.org/10.1093/hmg/ddi376 09646906 http://scholarbank.nus.edu.sg/handle/10635/150224 Oxford University Press Scopus |
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National University of Singapore |
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NUS Library |
| continent |
Asia |
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Singapore Singapore |
| content_provider |
NUS Library |
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ScholarBank@NUS |
| description |
10.1093/hmg/ddi376 |
| author2 |
DEPARTMENT OF COMPUTER SCIENCE |
| author_facet |
DEPARTMENT OF COMPUTER SCIENCE Skipper L. Li Y. Bonnard C. Pavanni R. Yih Y. Chua E. Sung W.-K. Tan L. Wong M.-C. Tan E.-K. Liu J. |
| format |
Article |
| author |
Skipper L. Li Y. Bonnard C. Pavanni R. Yih Y. Chua E. Sung W.-K. Tan L. Wong M.-C. Tan E.-K. Liu J. |
| spellingShingle |
Skipper L. Li Y. Bonnard C. Pavanni R. Yih Y. Chua E. Sung W.-K. Tan L. Wong M.-C. Tan E.-K. Liu J. Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease |
| author_sort |
Skipper L. |
| title |
Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease |
| title_short |
Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease |
| title_full |
Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease |
| title_fullStr |
Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease |
| title_full_unstemmed |
Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease |
| title_sort |
comprehensive evaluation of common genetic variation within lrrk2 reveals evidence for association with sporadic parkinson's disease |
| publisher |
Oxford University Press |
| publishDate |
2018 |
| url |
http://scholarbank.nus.edu.sg/handle/10635/150224 |
| _version_ |
1821222911418040320 |