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Gene mutational analysis in a cohort of Chinese children with unexplained epilepsy:identification of a new KCND3 phenotype and novel genes causing Dravet syndrome
Wang, Jiaping, Wen, Yongxin, Zhang, Qingping, Yu, Shujie, Chen, Yan, Wu, Xiru, Zhang, YueHua, Bao, XinhuaLanguage:
english
Journal:
Seizure
DOI:
10.1016/j.seizure.2019.01.025
Date:
January, 2019
File:
PDF, 428 KB
english, 2019