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A Chinese CADASIL family with p.R578C mutation at exon 11 of the NOTCH3 gene.
Wu, XuLing; Zhang, AnNi; Li, Ya; Lei, XiaoYang; Guo, ShiPeng; Tian, Tian; Gong, HuiLan; He, Dian.
Afiliação
  • Wu X; Department of Neurology, Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou Province, China.
  • Zhang A; Department of Neurology, Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou Province, China.
  • Li Y; Department of Neurology, Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou Province, China.
  • Lei X; Department of Neurology, Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou Province, China.
  • Guo S; Department of Neurology, Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou Province, China.
  • Tian T; Department of Neurology, Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou Province, China.
  • Gong H; Department of Neurology, Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou Province, China.
  • He D; Department of Neurology, Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou Province, China. Electronic address: hedian@gmc.edu.cn.
Clin Neurol Neurosurg ; 208: 106833, 2021 Sep.
Article em En | MEDLINE | ID: mdl-34352628

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: CADASIL / Receptor Notch3 / Mutação Tipo de estudo: Guideline / Risk_factors_studies Limite: Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Revista: Clin Neurol Neurosurg Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: CADASIL / Receptor Notch3 / Mutação Tipo de estudo: Guideline / Risk_factors_studies Limite: Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Revista: Clin Neurol Neurosurg Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China