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CHD4 variants are associated with childhood idiopathic epilepsy with sinus arrhythmia
CNS Neuroscience & Therapeutics ( IF 4.8 ) Pub Date : 2021-06-09 , DOI: 10.1111/cns.13692
Xiao-Rong Liu 1 , Ting-Ting Ye 1 , Wen-Jun Zhang 1 , Xuan Guo 1 , Jie Wang 1 , Shao-Ping Huang 2 , Long-Shan Xie 3 , Xing-Wang Song 1 , Wei-Wen Deng 1 , Bing-Mei Li 1 , Na He 1 , Qian-Yi Wu 1 , Min-Zhi Zhuang 1 , Meng Xu 1 , Yi-Wu Shi 1 , Tao Su 1 , Yong-Hong Yi 1 , Wei-Ping Liao 1 ,
Affiliation  

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.

中文翻译:

CHD4 变异与儿童特发性癫痫伴窦性心律失常有关

CHD4 基因编码染色体解旋酶DNA结合蛋白4,是胎儿发育的重要基因。在这项研究中,我们旨在探讨CHD4变异与特发性癫痫之间的关联。
更新日期:2021-06-09
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