A novel mutation in a common pathogenic gene (<i>SETD5</i>) associated with intellectual disability: A case report.

Fang, Yu-Lian; Zhang, Rui-Ping; Wang, Yi-Zheng; Cao, Li-Rong; Zhang, Yu-Qin; Cai, Chun-Quan

A novel mutation in a common pathogenic gene (SETD5) associated with intellectual disability: A case report.

Fang, Yu-Lian; Zhang, Rui-Ping; Wang, Yi-Zheng; Cao, Li-Rong; Zhang, Yu-Qin; Cai, Chun-Quan.

Afiliação

Fang YL; Institute of Pediatrics, Tianjin Children's Hospital, Tianjin 300134, P.R. China.
Zhang RP; Graduate College of Tianjin Medical University, Tianjin 300070, P.R. China.
Wang YZ; Graduate College of Tianjin Medical University, Tianjin 300070, P.R. China.
Cao LR; Graduate College of Tianjin Medical University, Tianjin 300070, P.R. China.
Zhang YQ; Department of Neurology, Tianjin Children's Hospital, Tianjin 300134, P.R. China.
Cai CQ; Department of Neurosurgery, Tianjin Children's Hospital, Tianjin 300134, P.R. China.

Exp Ther Med ; 18(5): 3737-3740, 2019 Nov.

Article em En | MEDLINE | ID: mdl-31656537

Palavras-chave

SETD5 gene; developmental delay; intellectual disability; whole exome sequencing

Texto completo

Adicionar na Minha BVS

Imprimir

XML

PubMed Links

Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Exp Ther Med Ano de publicação: 2019 Tipo de documento: Article País de publicação: Grécia

Texto completo

Adicionar na Minha BVS

Imprimir

XML

PubMed Links

Buscar no Google