CHD4 variants are associated with childhood idiopathic epilepsy with sinus arrhythmia

AIMS: CHD4 gene, encoding chromodomain helicase DNA‐binding protein 4, is a vital gene for fetal development. In this study, we aimed to explore the association between CHD4 variants and idiopathic epilepsy. METHODS: Trios‐based whole‐exome sequencing was performed in a cohort of 482 patients with c...

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Detalles Bibliográficos
Autores principales: Liu, Xiao‐Rong, Ye, Ting‐Ting, Zhang, Wen‐Jun, Guo, Xuan, Wang, Jie, Huang, Shao‐Ping, Xie, Long‐Shan, Song, Xing‐Wang, Deng, Wei‐Wen, Li, Bing‐Mei, He, Na, Wu, Qian‐Yi, Zhuang, Min‐Zhi, Xu, Meng, Shi, Yi‐Wu, Su, Tao, Yi, Yong‐Hong, Liao, Wei‐Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8446219/
https://www.ncbi.nlm.nih.gov/pubmed/34109749
http://dx.doi.org/10.1111/cns.13692

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8446219/
https://www.ncbi.nlm.nih.gov/pubmed/34109749
http://dx.doi.org/10.1111/cns.13692

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