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Article

SNCA rs356182 variant increases risk of sporadic Parkinson's disease in ethnic Chinese.

Journal of the neurological sciences - 15 Sept 2016

Cheng Lan, Wang Ling, Li Nan-Nan, Yu Wen-Juan, Sun Xiao-Yi, Li Jun-Ying, Zhou Dong, Peng Rong

Abstract excerpt

PURPOSE: A genome-wide association study (GWAS) has recently identified a novel single nucleotide polymorphism (SNP) rs356182 at SNCA that can modulate the risk of Parkinson's disease (PD) in Caucasian ancestry. The present study was designed to clarify the strength of the association in ethnic Chinese population. METHODS: Using a case-control methodology, we genotyped the SNP rs356182 to investigate the...

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Identifiers

PMID: 27538639
DOI: 10.1016/j.jns.2016.07.032

Genes

SNCA

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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