Correlation of SV2C rs1423099 single nucleotide polymorphism with sporadic Parkinson's disease in Han population in Southern China.

Tan, Zixin; Lin, Yuwan; Zhou, Miaomiao; Guo, Wenyuan; Qiu, Jiewen; Ding, Liuyan; Wu, Zhuohua; Xu, Pingyi; Chen, Xiang

Tan, Zixin; Lin, Yuwan; Zhou, Miaomiao; Guo, Wenyuan; Qiu, Jiewen; Ding, Liuyan; Wu, Zhuohua; Xu, Pingyi; Chen, Xiang.

Afiliação

Tan Z; Department of Neurology, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510120, China.
Lin Y; Department of Neurology, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510120, China.
Zhou M; Department of Neurology, Shanghai General Hospital, Shanghai 200940, China.
Guo W; Department of Neurology, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510120, China.
Qiu J; Department of Neurology, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510120, China.
Ding L; Department of Neurology, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510120, China.
Wu Z; Department of Neurology, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510120, China. Electronic address: zhh88w@126.com.
Xu P; Department of Neurology, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510120, China. Electronic address: pingyixu@sina.com.
Chen X; Department of Neurology, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510120, China. Electronic address: wuliancx@163.com.

Neurosci Lett ; 813: 137426, 2023 09 14.

Article em En | MEDLINE | ID: mdl-37544580

Assuntos

Doença de Parkinson; Polimorfismo de Nucleotídeo Único; Humanos; Masculino; Estudos de Casos e Controles; China; Frequência do Gene; Predisposição Genética para Doença/genética; Genótipo; Glicoproteínas de Membrana/genética; Proteínas do Tecido Nervoso/genética; Doença de Parkinson/genética; Feminino

Palavras-chave

Parkinson's disease; SV2C; Single nucleotide polymorphism; rs1423099

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Polimorfismo de Nucleotídeo Único Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Female / Humans / Male País/Região como assunto: Asia Idioma: En Ano de publicação: 2023 Tipo de documento: Article

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