Browsing by Author Yu, Shujie
Showing results 1 to 4 of 4
Issue Date | Title | Author(s) |
2019 | 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, Xinhua |
2019 | Genomic mosaicism in the pathogenesis and inheritance of a Rett syndrome cohort | Zhang, Qingping; Yang, Xiaoxu; Wang, Jiaping; Li, Jiarui; Wu, Qixi; Wen, Yongxin; Zhao, Ying; Zhang, Xiaoying; Yao, He; Wu, Xiru; Yu, Shujie; Wei, Liping; Bao, Xinhua |
2019 | Genomic mosaicism in the pathogenesis and inheritance of a Rett syndrome cohort (vol 21, pg 1330, 2019) | Zhang, Qingping; Yang, Xiaoxu; Wang, Jiaping; Li, Jiarui; Wu, Qixi; Wen, Yongxin; Zhao, Ying; Zhang, Xiaoying; Yao, He; Wu, Xiru; Yu, Shujie; Wei, Liping; Bao, Xinhua |
2017 | SCN8A mutations in Chinese patients with early onset epileptic encephalopathy and benign infantile seizures | Wang, Jiaping; Gao, Hua; Bao, Xinhua; Zhang, Qingping; Li, Jiarui; Wei, Liping; Wu, Xiru; Chen, Yan; Yu, Shujie |