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Polymorphism in MIR4697 but not VPS13C, GCH1, or SIPA1L2 is associated with risk of Parkinson's disease in a Han Chinese population.
Yang, Xinglong; Zheng, Jinhua; An, Ran; Tian, Sijia; Zhao, Quanzhen; Chen, Yalan; Huang, Hongyan; Ning, Ping Ping; Song, Yi; Xu, Yanming.
Afiliación
  • Yang X; Department of Neurology, West China Hospital, Sichuan University, 37 Guo Xue Xiang, Chengdu, Sichuan Province, 610041, PR China; Department of Geriatric Neurology, First Affiliated Hospital of Kunming Medical University, Kunming, Yunan Province, 650032, PR China.
  • Zheng J; Department of Neurology, West China Hospital, Sichuan University, 37 Guo Xue Xiang, Chengdu, Sichuan Province, 610041, PR China.
  • An R; Department of Neurology, West China Hospital, Sichuan University, 37 Guo Xue Xiang, Chengdu, Sichuan Province, 610041, PR China.
  • Tian S; Department of Neurology, West China Hospital, Sichuan University, 37 Guo Xue Xiang, Chengdu, Sichuan Province, 610041, PR China.
  • Zhao Q; Department of Neurology, West China Hospital, Sichuan University, 37 Guo Xue Xiang, Chengdu, Sichuan Province, 610041, PR China.
  • Chen Y; Department of Neurology, West China Hospital, Sichuan University, 37 Guo Xue Xiang, Chengdu, Sichuan Province, 610041, PR China.
  • Huang H; Department of Neurology, West China Hospital, Sichuan University, 37 Guo Xue Xiang, Chengdu, Sichuan Province, 610041, PR China.
  • Ning PP; Department of Neurology, West China Hospital, Sichuan University, 37 Guo Xue Xiang, Chengdu, Sichuan Province, 610041, PR China.
  • Song Y; Department of Pharmacy, West China Hospital, Sichuan University, Chengdu, Sichuan 610041, PR China. Electronic address: syi@scu.edu.cn.
  • Xu Y; Department of Neurology, West China Hospital, Sichuan University, 37 Guo Xue Xiang, Chengdu, Sichuan Province, 610041, PR China. Electronic address: neuroxym999@163.com.
Neurosci Lett ; 650: 8-11, 2017 05 22.
Article en En | MEDLINE | ID: mdl-28380328
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Proteínas / Predisposición Genética a la Enfermedad / Polimorfismo de Nucleótido Simple / MicroARNs Tipo de estudio: Diagnostic_studies / Etiology_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Neurosci Lett Año: 2017 Tipo del documento: Article Pais de publicación: Irlanda
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Proteínas / Predisposición Genética a la Enfermedad / Polimorfismo de Nucleótido Simple / MicroARNs Tipo de estudio: Diagnostic_studies / Etiology_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Neurosci Lett Año: 2017 Tipo del documento: Article Pais de publicación: Irlanda