Genetic and Phenotype Analysis of a Chinese Cohort of Infants and Children With Epilepsy.

Chuan, Zhang; Ruikun, Cai; Qian, Li; Shiyue, Mei; Shengju, Hao; Yong, Yuan; Haibo, Li; Neng, Xiao; Yong, Zhao; Huiqin, Xue; Weijia, Wang; Ling, Hui; Bingbo, Zhou; Zhang, Qinghua; Yan, Wang; Zongfu, Cao; Xu, Ma

Chuan, Zhang; Ruikun, Cai; Qian, Li; Shiyue, Mei; Shengju, Hao; Yong, Yuan; Haibo, Li; Neng, Xiao; Yong, Zhao; Huiqin, Xue; Weijia, Wang; Ling, Hui; Bingbo, Zhou; Zhang, Qinghua; Yan, Wang; Zongfu, Cao; Xu, Ma.

Afiliación

Chuan Z; National Research Institute for Family Planning, National Human Genetic Resources Center, Beijing, China.
Ruikun C; Gansu Province Medical Genetics Center, Gansu Provincial Clinical Research Center for Birth Defects and Rare Diseases, Gansu Provincial Maternity and Child-Care Hospital, Lanzhou, China.
Qian L; Graduate School of Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, China.
Shiyue M; National Research Institute for Family Planning, National Human Genetic Resources Center, Beijing, China.
Shengju H; National Research Institute for Family Planning, National Human Genetic Resources Center, Beijing, China.
Yong Y; Department of Intensive Care Unit, Henan Provincial Key Laboratory of Children's Genetics and Metabolic Diseases, Children's Hospital Affiliated to Zhengzhou University, Zhengzhou, China.
Haibo L; Gansu Province Medical Genetics Center, Gansu Provincial Clinical Research Center for Birth Defects and Rare Diseases, Gansu Provincial Maternity and Child-Care Hospital, Lanzhou, China.
Neng X; Zhongshan City People's Hospital, Affiliated Zhongshan Hospital of Sun Yat-Sen University, Guangzhou, China.
Yong Z; The Central Laboratory of Birth Defects Prevention and Control, Ningbo Women and Children's Hospital, Ningbo, China.
Huiqin X; Department of Pediatric Neurology, Chenzhou First People's Hospital, Chenzhou, China.
Weijia W; Foshan Women and Children Hospital, Foshan, China.
Ling H; Children's Hospital of Shanxi, Women Health Center of Shanxi, Taiyuan, China.
Bingbo Z; Zhongshan City People's Hospital, Affiliated Zhongshan Hospital of Sun Yat-Sen University, Guangzhou, China.
Zhang Q; Gansu Province Medical Genetics Center, Gansu Provincial Clinical Research Center for Birth Defects and Rare Diseases, Gansu Provincial Maternity and Child-Care Hospital, Lanzhou, China.
Yan W; Gansu Province Medical Genetics Center, Gansu Provincial Clinical Research Center for Birth Defects and Rare Diseases, Gansu Provincial Maternity and Child-Care Hospital, Lanzhou, China.
Zongfu C; Gansu Province Medical Genetics Center, Gansu Provincial Clinical Research Center for Birth Defects and Rare Diseases, Gansu Provincial Maternity and Child-Care Hospital, Lanzhou, China.
Xu M; Gansu Province Medical Genetics Center, Gansu Provincial Clinical Research Center for Birth Defects and Rare Diseases, Gansu Provincial Maternity and Child-Care Hospital, Lanzhou, China.

Front Genet ; 13: 869210, 2022.

Article en En | MEDLINE | ID: mdl-35571021

Palabras clave

WES; genetics counseling; infant and children epilepsy; phenotypes; variant

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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Front Genet Año: 2022 Tipo del documento: Article País de afiliación: China