Human Genome Epidemiology Literature Finder
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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. Seizure 2019 2 66 26-30. Wang Jiaping, Wen Yongxin, Zhang Qingping, Yu Shujie, Chen Yan, Wu Xiru, Zhang YueHua, Bao Xinh |
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- Page last updated:May 06, 2024
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