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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Bibliographic Details
Main Authors: 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.
Other Authors: DUKE-NUS MEDICAL SCHOOL
Format: Article
Published: Oxford University Press 2018
Online Access:http://scholarbank.nus.edu.sg/handle/10635/150224
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Institution: National University of Singapore
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spelling sg-nus-scholar.10635-1502242024-04-25T06:34:20Z 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. DUKE-NUS MEDICAL SCHOOL DEPARTMENT OF COMPUTER SCIENCE GENOME INSTITUTE OF SINGAPORE 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
institution National University of Singapore
building NUS Library
continent Asia
country Singapore
Singapore
content_provider NUS Library
collection ScholarBank@NUS
description 10.1093/hmg/ddi376
author2 DUKE-NUS MEDICAL SCHOOL
author_facet DUKE-NUS MEDICAL SCHOOL
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
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