Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease-Reference-Cited by-同舟云学术

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Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease

Published:2005-11-03 Issue:23 Volume:14 Page:3549-3556
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Skipper Lisa,Li Yi,Bonnard Carine,Pavanni Ratnagopal,Yih Yuen,Chua Eva,Sung Wing-Kin,Tan Louis,Wong Meng-Cheong,Tan Eng-King,Liu Jianjun

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/14/23/3549/1489964/ddi376.pdf

Reference34 articles.

1. Rocca, W.A. (2005) Prevalence of Parkinson's disease in China. Lancet Neurol., 4, 328–329.

2. Gelb, D.J., Oliver, E. and Gilman, S. (1999) Diagnostic criteria for Parkinson disease. Arch. Neurol., 56, 33–39.

3. Forno, L.S. (1996) Neuropathology of Parkinson's disease. J. Neuropathol. Exp. Neurol., 55, 259–272.

4. Vila, M. and Przedborski, S. (2004) Genetic clues to the pathogenesis of Parkinson's disease. Nat. Med., 10 (suppl.), S58–S62.

5. Polymeropoulos, M.H., Lavedan, C., Leroy, E., Ide, S.E., Dehejia, A., Dutra, A., Pike, B., Root, H., Rubenstein, J., Boyer, R. et al. (1997) Mutation in the alpha-synuclein gene identified in families with Parkinson's disease. Science, 276, 2045–2047.

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