Literature DB >> 27084066

MC1R variants in Chinese Han patients with sporadic Parkinson's disease.

Chang-He Shi1, Hui Wang2, Cheng-Yuan Mao2, Jing Yang1, Bo Song1, Yu-Tao Liu1, Zhi-Hua Yang1, Hai-Yang Luo2, Shu-Yu Zhang2, Jun Wu1, Yu-Ming Xu3.   

Abstract

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.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Association; Chinese population; MC1R; Parkinson's disease; Variant

Mesh:

Substances:

Year:  2016        PMID: 27084066     DOI: 10.1016/j.neurobiolaging.2016.02.026

Source DB:  PubMed          Journal:  Neurobiol Aging        ISSN: 0197-4580            Impact factor:   4.673


  4 in total

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3.  Genetic analysis of the TMEM230 gene in Chinese Han patients with Parkinson's disease.

Authors:  Chang-He Shi; Fang Li; Meng-Meng Shi; Zhi-Hua Yang; Cheng-Yuan Mao; Shu-Yu Zhang; Hui Wang; Yuan Cheng; Jing Yang; Jun Wu; Yu-Ming Xu
Journal:  Sci Rep       Date:  2017-04-26       Impact factor: 4.379

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  4 in total

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