Treating GNAO1 mutation-related severe movement disorders with oxcarbazepine: a case report

por Ling, Weihao, Huang, Danping, Yang, Fan, Yang, Zuozhen, Liu, Min, Zhu, Qiujiao, Huang, Jing, Zhou, Rui, Chen, Xuqin
Publicado 2022

De novo ATP1A2 variants in two Chinese children with alternating hemiplegia of childhood upgraded the gene–disease relationship and variant classification: a case report

por Huang, Danping, Liu, Min, Wang, Hongying, Zhang, Bingbing, Zhao, Dongjing, Ling, Weihao, Wang, Manli, Feng, Jun, Shen, Yiping, Chen, Xuqin
Publicado 2021