Browsing by Author Ding, Changhong
Showing results 1 to 4 of 4
Issue Date | Title | Author(s) |
2019 | Altered inhibitory synapses in de novo GABRA5 and GABRA1 mutations associated with early onset epileptic encephalopathies | Hernandez, Ciria C.; XiangWei, Wenshu; Hu, Ningning; Shen, Dingding; Shen, Wangzhen; Lagrange, Andre H.; Zhang, Yujia; Dai, Lifang; Ding, Changhong; Sun, Zhaohui; Hu, Jiasheng; Zhu, Hongmin; Jiang, Yuwu; Macdonald, Robert L. |
Jul-2021 | Genotype-phenotype correlation of CACNA1A variants in children with epilepsy | Niu, Xueyang; Yang, Ying; Chen, Yi; Cheng, Miaomiao; Liu, Ming; Ding, Changhong; Tian, Xiaojuan; Yang, Zhixian; Jiang, Yuwu; Zhang, Yuehua |
2011 | Identification of novel MLC1 mutations in Chinese patients with megalencephalic leukoencephalopathy with subcortical cysts (MLC) | Wang, Jingmin; Shang, Jing; Wu, Ye; Gu, Qiang; Xiong, Hui; Ding, Changhong; Wang, Liwen; Gao, Zhijie; Wu, Xiru; Jiang, Yuwu |
2017 | Molecular spectrum of excision repair cross-complementation group 8 gene defects in Chinese patients with Cockayne syndrome type A | Wang, Xiaozhu; Huang, Yu; Yan, Ming; Li, Jiuwei; Ding, Changhong; Jin, Hong; Fang, Fang; Yang, Yanling; Wu, Baiyan; Chen, Dafang |