Your browser doesn't support javascript.
loading
[Genetics Analysis of patients with Dravet syndrome due to mosaicism variation of paternal SCN1A gene].
Huo, M Z; Niu, W B; Xu, J W; Shi, H; Liu, Y D; Zhang, Y L.
Afiliação
  • Huo MZ; Center for Reproductive Medicine(Henan Key Laboratory of Reproduction and Genetics), the First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.
  • Niu WB; Center for Reproductive Medicine(Henan Key Laboratory of Reproduction and Genetics), the First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.
  • Xu JW; Center for Reproductive Medicine(Henan Key Laboratory of Reproduction and Genetics), the First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.
  • Shi H; Center for Reproductive Medicine(Henan Key Laboratory of Reproduction and Genetics), the First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.
  • Liu YD; Center for Reproductive Medicine(Henan Key Laboratory of Reproduction and Genetics), the First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.
  • Zhang YL; Center for Reproductive Medicine(Henan Key Laboratory of Reproduction and Genetics), the First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.
Zhonghua Yi Xue Za Zhi ; 101(16): 1182-1185, 2021 Apr 27.
Article em Zh | MEDLINE | ID: mdl-33902251
Assuntos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Espasmos Infantis / Epilepsias Mioclônicas Idioma: Zh Ano de publicação: 2021 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Espasmos Infantis / Epilepsias Mioclônicas Idioma: Zh Ano de publicação: 2021 Tipo de documento: Article