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Gene mutational analysis in a cohort of Chinese children with unexplained epilepsy: Identification of a new KCND3 phenotype and novel genes causing Dravet syndrome.
Wang, Jiaping; Wen, Yongxin; Zhang, Qingping; Yu, Shujie; Chen, Yan; Wu, Xiru; Zhang, YueHua; Bao, Xinhua.
Afiliação
  • Wang J; Department of Pediatrics, Peking University First Hospital, Beijing 100034, China.
  • Wen Y; Department of Pediatrics, Peking University First Hospital, Beijing 100034, China.
  • Zhang Q; Department of Pediatrics, Peking University First Hospital, Beijing 100034, China.
  • Yu S; Department of Neurology, Harbin Children's Hospital, Harbin 150010, Heilongjiang Province, China.
  • Chen Y; Department of Pediatrics, Peking University First Hospital, Beijing 100034, China.
  • Wu X; Department of Pediatrics, Peking University First Hospital, Beijing 100034, China.
  • Zhang Y; Department of Pediatrics, Peking University First Hospital, Beijing 100034, China.
  • Bao X; Department of Pediatrics, Peking University First Hospital, Beijing 100034, China. Electronic address: zwhang@pku.edu.cn.
Seizure ; 66: 26-30, 2019 Mar.
Article em En | MEDLINE | ID: mdl-30776697

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Epilepsias Mioclônicas / Canais de Potássio Shal / Mutação Tipo de estudo: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Child, preschool / Female / Humans / Infant / Male País/Região como assunto: Asia Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Epilepsias Mioclônicas / Canais de Potássio Shal / Mutação Tipo de estudo: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Child, preschool / Female / Humans / Infant / Male País/Região como assunto: Asia Idioma: En Ano de publicação: 2019 Tipo de documento: Article