PRRT2 gene mutations associated with infantile convulsions induced by sucking and the genotype-phenotype correlation

por Liu, De-Tian, Tang, Xue-Qing, Wan, Rui-Ping, Luo, Sheng, Guan, Bao-Zhu, Li, Bin, Liu, Li-Hong, Li, Bing-Mei, Liu, Zhi-Gang, Xie, Long-Shan, Yi, Yong-Hong
Publicado 2022

SZT2 variants associated with partial epilepsy or epileptic encephalopathy and the genotype-phenotype correlation

por Luo, Sheng, Ye, Xing-Guang, Jin, Liang, Li, Huan, He, Yun-Yan, Guan, Bao-Zhu, Gao, Liang-Di, Liang, Xiao-Yu, Wang, Peng-Yu, Lu, Xin-Guo, Yan, Hong-Jun, Li, Bing-Mei, Chen, Yong-Jun, Liu, Zhi-Gang
Publicado 2023

HLA Risk Alleles in Aromatic Antiepileptic Drug-Induced Maculopapular Exanthema

por Shi, Yi-Wu, Wang, Jie, Min, Fu-Li, Bian, Wen-Jun, Mao, Bi-Jun, Mao, Yong, Qin, Bing, Li, Bing-Mei, Ou, Yang-Mei, Hou, Yun-Qi, Zou, Xin, Guan, Bao-Zhu, He, Na, Chen, Yong-Jun, Li, Xue-Lian, Wang, Juan, Deng, Wei-Yi, Liu, Han-Kui, Shen, Nan-Xiang, Liu, Xiao-Rong, Yi, Yong-Hong, Zhou, Lie-Min, Zhou, Dong, Kwan, Patrick, Liao, Wei-Ping
Publicado 2021

HCFC1 variants in the proteolysis domain are associated with X‐linked idiopathic partial epilepsy: Exploring the underlying mechanism

por He, Na, Guan, Bao‐Zhu, Wang, Jie, Liu, Han‐Kui, Mao, Yong, Liu, Zhi‐Gang, Yin, Fei, Peng, Jing, Xiao, Bo, Tang, Bei‐sha, Zhou, Dong, Huang, Guang, Dai, Qi‐Lin, Zeng, Ying, Han, Hong, Zhai, Qiong‐Xiang, Li, Bin, Tang, Bin, Li, Wen‐Bin, Song, Wang, Liu, Liu, Shi, Yi‐Wu, Li, Bing‐Mei, Su, Tao, Zhou, Peng, Liu, Xiao‐Rong, Guo, Li‐Wu, Yi, Yong‐Hong, Liao, Wei‐Ping
Publicado 2023