SNCA rs356182 Variant Increases Risk of Sporadic Parkinson's Disease in Ethnic Chinese

Abstract 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 i...

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Veröffentlicht in:	Journal of the neurological sciences 2016-09, Vol.368, p.231-234
Hauptverfasser:	Cheng, Lan, Wang, Ling, Li, Nan-Nan, Yu, Wen-Juan, Sun, Xiao-Yi, Li, Jun-Ying, Zhou, Dong, Peng, Rong
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Aged Aged, 80 and over Alpha-synuclein alpha-Synuclein - genetics Asian Continental Ancestry Group - ethnology Asian Continental Ancestry Group - genetics Case-Control Studies Female Gene Frequency Genetic Predisposition to Disease Genome-Wide Association Study Humans Male Middle Aged Neurology Parkinson Disease - epidemiology Parkinson Disease - ethnology Parkinson Disease - genetics Parkinson's disease Polymorphism, Single Nucleotide - genetics Single nucleotide polymorphism Young Adult
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