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Novel TARDBP missense mutation caused familial amyotrophic lateral sclerosis with frontotemporal dementia and parkinsonism.
Chen, Sheng; Zhou, Rui-Ling; Zhang, Wei; Che, Chun-Hui; Feng, Shu-Yan; Huang, Hua-Pin; Liu, Chang-Yun; Zou, Zhang-Yu.
Afiliação
  • Chen S; Department of Neurology, Fujian Medical University Union Hospital, Fuzhou, China; Institute of Clinical Neurology, Fujian Medical University, Fuzhou, China.
  • Zhou RL; Department of Neurology, Fujian Provincial Hospital, Fuzhou, China.
  • Zhang W; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX; AmCare Genomics Lab, Guangzhou, China.
  • Che CH; Department of Neurology, Fujian Medical University Union Hospital, Fuzhou, China.
  • Feng SY; Department of Neurology, Henan Provincial People's Hospital, Zhengzhou, China.
  • Huang HP; Department of Neurology, Fujian Medical University Union Hospital, Fuzhou, China; Institute of Clinical Neurology, Fujian Medical University, Fuzhou, China.
  • Liu CY; Department of Neurology, Fujian Medical University Union Hospital, Fuzhou, China; Institute of Clinical Neurology, Fujian Medical University, Fuzhou, China. Electronic address: changyunliu@fjmu.edu.cn.
  • Zou ZY; Department of Neurology, Fujian Medical University Union Hospital, Fuzhou, China; Institute of Clinical Neurology, Fujian Medical University, Fuzhou, China. Electronic address: fmuzzy@fjmu.edu.cn.
Neurobiol Aging ; 107: 168-173, 2021 11.
Article em En | MEDLINE | ID: mdl-34175147
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Mutação de Sentido Incorreto / Transtornos Parkinsonianos / Proteínas de Ligação a DNA / Demência Frontotemporal / Esclerose Lateral Amiotrófica Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Mutação de Sentido Incorreto / Transtornos Parkinsonianos / Proteínas de Ligação a DNA / Demência Frontotemporal / Esclerose Lateral Amiotrófica Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Ano de publicação: 2021 Tipo de documento: Article