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Somatic variants in new candidate genes identified in focal cortical dysplasia type II.
Zhang, Zhongbin; Gao, Kai; Liu, Qingzhu; Zhou, Jiapeng; Li, Xiyuan; Lang, Na; Liu, Ming; Wang, Tianshuang; Zhang, Jie; Wang, Hui; Dong, Ying; Ji, Taoyun; Wang, Shuang; Liu, Xiaoyan; Jiang, Yuwu; Cai, Lixin; Wu, Ye.
Afiliación
  • Zhang Z; Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Gao K; Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Liu Q; Pediatric Epilepsy Center, Peking University First Hospital, Beijing, China.
  • Zhou J; College of Life Sciences, Hunan Normal University, Changsha, China.
  • Li X; Institute of Computing Technology, Chinese Academy of Science, Beijing, China.
  • Lang N; College of Life Sciences, Hunan Normal University, Changsha, China.
  • Liu M; Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Wang T; Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Zhang J; Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Wang H; Department of Pathology, Peking University First Hospital, Beijing, China.
  • Dong Y; Department of Pathology, Peking University First Hospital, Beijing, China.
  • Ji T; Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Wang S; Pediatric Epilepsy Center, Peking University First Hospital, Beijing, China.
  • Liu X; Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Jiang Y; Pediatric Epilepsy Center, Peking University First Hospital, Beijing, China.
  • Cai L; Department of Pediatrics, Peking University First Hospital, Beijing, China.
  • Wu Y; Pediatric Epilepsy Center, Peking University First Hospital, Beijing, China.
Epilepsia ; 61(4): 667-678, 2020 04.
Article en En | MEDLINE | ID: mdl-32216069
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Epilepsia / Malformaciones del Desarrollo Cortical de Grupo I Límite: Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Epilepsia Año: 2020 Tipo del documento: Article País de afiliación: China
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Epilepsia / Malformaciones del Desarrollo Cortical de Grupo I Límite: Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Epilepsia Año: 2020 Tipo del documento: Article País de afiliación: China