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Meta-analysis of the association between ZNF512B polymorphism rs2275294 and risk of amyotrophic lateral sclerosis.
Ning, Pingping; Yang, Xinglong; Yang, Baiyuan; Zhao, Quanzhen; Huang, Hongyan; An, Ran; Chen, Yalan; Hu, Fayun; Xu, Zhuping; Xu, Yanming.
Afiliación
  • Ning P; Department of Neurology, West China Hospital, Sichuan University, 37 Guo Xue Xiang, Chengdu, Sichuan Province, 610041, People's Republic of China.
  • Yang X; Department of Geriatric Neurology, First Affiliated Hospital of Kunming Medical University, 295 Xi Change Road, Kunming, 650032, Yunnan Province, People's Republic of China.
  • Yang B; Department of Neurology, Seventh People's Hospital of Chengdu, Chengdu, Sichuan Province, People's Republic of China.
  • Zhao Q; Department of Neurology, West China Hospital, Sichuan University, 37 Guo Xue Xiang, Chengdu, Sichuan Province, 610041, People's Republic of China.
  • Huang H; Department of Neurology, West China Hospital, Sichuan University, 37 Guo Xue Xiang, Chengdu, Sichuan Province, 610041, People's Republic of China.
  • An R; Department of Neurology, West China Hospital, Sichuan University, 37 Guo Xue Xiang, Chengdu, Sichuan Province, 610041, People's Republic of China.
  • Chen Y; Department of Neurology, West China Hospital, Sichuan University, 37 Guo Xue Xiang, Chengdu, Sichuan Province, 610041, People's Republic of China.
  • Hu F; Department of Neurology, West China Hospital, Sichuan University, 37 Guo Xue Xiang, Chengdu, Sichuan Province, 610041, People's Republic of China.
  • Xu Z; Department of Ophthalmology, West China Hospital, Sichuan University, Chengdu, Sichuan Province, People's Republic of China. zhuping_xu@yahoo.com.
  • Xu Y; Department of Neurology, West China Hospital, Sichuan University, 37 Guo Xue Xiang, Chengdu, Sichuan Province, 610041, People's Republic of China. neuroxym999@163.com.
Neurol Sci ; 39(7): 1261-1266, 2018 Jul.
Article en En | MEDLINE | ID: mdl-29713939

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Proteínas Portadoras / Predisposición Genética a la Enfermedad / Polimorfismo de Nucleótido Simple / Esclerosis Amiotrófica Lateral Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Humans Idioma: En Revista: Neurol Sci Asunto de la revista: NEUROLOGIA Año: 2018 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Proteínas Portadoras / Predisposición Genética a la Enfermedad / Polimorfismo de Nucleótido Simple / Esclerosis Amiotrófica Lateral Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Humans Idioma: En Revista: Neurol Sci Asunto de la revista: NEUROLOGIA Año: 2018 Tipo del documento: Article