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首页> 外文期刊>Neurobiology of Aging: Experimental and Clinical Research >MC1R variants in Chinese Han patients with sporadic Parkinson's disease
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MC1R variants in Chinese Han patients with sporadic Parkinson's disease

机译:中国汉族散发性帕金森病患者的MC1R变异

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摘要

Recently, a variant p.R160W in the MC1R gene was identified that increased the risk of Parkinson's disease (PD) in Spanish population. To explore whether the MC1R gene variants are associated with sporadic PD in Chinese population, we performed a case-control comparison study for comprehensive MC1R variant screening in 510 Chinese Han patients and 495 healthy controls as ethnically matched controls. We identify 5 nonsynonymous variants, including rs34090186 (p.R67Q), rs2228479 (p.V92M), rs33932559 (p.I120T), rs885479 (p.R163Q), and rs372152373 (p.R223W). However, variants mentioned previously did not show association with PD. Our results suggest that variants in MC1R do not play a major role in PD in the Chinese population. (C) 2016 Elsevier Inc. All rights reserved.
机译:最近,发现了MC1R基因中的p.R160W变异体,该变异体增加了西班牙人群帕金森氏病(PD)的风险。为了探讨中国人群中MC1R基因变异是否与散发性PD相关,我们进行了病例对照比较研究,对510名中国汉族患者和495名健康对照作为种族匹配对照进行了全面的MC1R变异筛查。我们确定了5个非同义变体,包括rs34090186(p.R67Q),rs2228479(p.V92M),rs33932559(p.I120T),rs885479(p.R163Q)和rs372152373(p.R223W)。但是,前面提到的变体没有显示与PD的关联。我们的结果表明,MC1R的变异体在中国人群的PD中不发挥主要作用。 (C)2016 Elsevier Inc.保留所有权利。

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