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A Heterozygous Variant of FGF13 Caused X-Linked Developmental and Epileptic Encephalopathy 90 in a Chinese Family.
Cheng, Haiying; Miao, Pu; Wang, Ye; Guo, Yufan; Gao, Liuyan; Lou, Yuting; Yang, Fan; Liang, Mengmeng; Feng, Jianhua.
Afiliação
  • Cheng H; Department of Paediatrics, The Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
  • Miao P; Department of Paediatrics, The Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
  • Wang Y; Department of Paediatrics, The Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
  • Guo Y; Department of Paediatrics, The Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
  • Gao L; Department of Paediatrics, The Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
  • Lou Y; Department of Paediatrics, The Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
  • Yang F; Cipher Gene LLC, Beijing, China.
  • Liang M; Cipher Gene LLC, Beijing, China.
  • Feng J; Department of Paediatrics, The Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Cytogenet Genome Res ; 163(1-2): 36-41, 2023.
Article em En | MEDLINE | ID: mdl-37536293
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Epilepsia / População do Leste Asiático Tipo de estudo: Guideline / Prognostic_studies Limite: Female / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Epilepsia / População do Leste Asiático Tipo de estudo: Guideline / Prognostic_studies Limite: Female / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article