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Burden of rare variants in ALS genes influences survival in familial and sporadic ALS.
Pang, Shirley Yin-Yu; Hsu, Jacob Shujui; Teo, Kay-Cheong; Li, Yan; Kung, Michelle H W; Cheah, Kathryn S E; Chan, Danny; Cheung, Kenneth M C; Li, Miaoxin; Sham, Pak-Chung; Ho, Shu-Leong.
Afiliación
  • Pang SY; Division of Neurology, Department of Medicine, University of Hong Kong, Hong Kong, P.R. China.
  • Hsu JS; Department of Psychiatry, University of Hong Kong, Hong Kong, P.R. China; Centre for Genomic Sciences, Li Ka Shing Faculty of Medicine, University of Hong Kong, Hong Kong, P.R. China.
  • Teo KC; Division of Neurology, Department of Medicine, University of Hong Kong, Hong Kong, P.R. China.
  • Li Y; Department of Psychiatry, University of Hong Kong, Hong Kong, P.R. China; Centre for Genomic Sciences, Li Ka Shing Faculty of Medicine, University of Hong Kong, Hong Kong, P.R. China.
  • Kung MHW; Division of Neurology, Department of Medicine, University of Hong Kong, Hong Kong, P.R. China.
  • Cheah KSE; School of Biomedical Sciences, Li Ka Shing Faculty of Medicine, University of Hong Kong, Hong Kong, P.R. China.
  • Chan D; School of Biomedical Sciences, Li Ka Shing Faculty of Medicine, University of Hong Kong, Hong Kong, P.R. China.
  • Cheung KMC; Department of Orthopaedics & Traumatology, University of Hong Kong, Hong Kong, P.R. China.
  • Li M; Department of Psychiatry, University of Hong Kong, Hong Kong, P.R. China; Centre for Genomic Sciences, Li Ka Shing Faculty of Medicine, University of Hong Kong, Hong Kong, P.R. China; Department of Medical Genetics, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, P.R. China; Key Lab
  • Sham PC; Department of Psychiatry, University of Hong Kong, Hong Kong, P.R. China; Centre for Genomic Sciences, Li Ka Shing Faculty of Medicine, University of Hong Kong, Hong Kong, P.R. China. Electronic address: pcsham@hku.hk.
  • Ho SL; Division of Neurology, Department of Medicine, University of Hong Kong, Hong Kong, P.R. China. Electronic address: slho@hku.hk.
Neurobiol Aging ; 58: 238.e9-238.e15, 2017 10.
Article en En | MEDLINE | ID: mdl-28709720
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Variación Genética / Estudios de Asociación Genética / Esclerosis Amiotrófica Lateral Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Neurobiol Aging Año: 2017 Tipo del documento: Article
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Variación Genética / Estudios de Asociación Genética / Esclerosis Amiotrófica Lateral Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Neurobiol Aging Año: 2017 Tipo del documento: Article