Gene Mutation Analysis in 253 Chinese Children with Unexplained Epilepsy and Intellectual/Developmental Disabilities

OBJECTIVE: Epilepsy and intellectual/developmental disabilities (ID/DD) have a high rate of co-occurrence. Here, we investigated gene mutations in Chinese children with unexplained epilepsy and ID/DD. METHODS: We used targeted next-generation sequencing to detect mutations within 300 genes related t...

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Detalles Bibliográficos
Autores principales: Zhang, Yujia, Kong, Weijing, Gao, Yang, Liu, Xiaoyan, Gao, Kai, Xie, Han, Wu, Ye, Zhang, Yuehua, Wang, Jingmin, Gao, Feng, Wu, Xiru, Jiang, Yuwu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4636363/
https://www.ncbi.nlm.nih.gov/pubmed/26544041
http://dx.doi.org/10.1371/journal.pone.0141782

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4636363/
https://www.ncbi.nlm.nih.gov/pubmed/26544041
http://dx.doi.org/10.1371/journal.pone.0141782

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