期刊
NEUROSCIENCE LETTERS
卷 442, 期 3, 页码 200-202出版社
ELSEVIER IRELAND LTD
DOI: 10.1016/j.neulet.2008.07.012
关键词
Parkinson's disease; UCHL1; S18Y; gene polymorphism
资金
- Science and Technology Bureau of Sichuan Province, PR China [2006J13-099]
Mutation in UCH-L1 has been reported as a rare cause of autosomal dominant Parkinson's disease (PD). A S18Y polymorphism in the same gene has been associated with sporadic PD. We investigated the frequency of this polymorphism among the Han-Chinese ethnic population in a case-control study. A total of 600 patients with PD and 334 unrelated healthy controls were genotyped using PCR-restriction fragment length polymorphism analysis. We did not observe any difference in allele or genotype frequencies between the cases and the controls (P > 0.05). Our results do not support a role for this variant in sporadic PD. (c) 2008 Elsevier Ireland Ltd. All rights reserved.
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