Genetic (idiopathic) epilepsy with photosensitive seizures includes features of both focal and generalized seizures

Por Xue, Jiao, Gong, Pan, Yang, Haipo, Liu, Xiaoyan, Jiang, Yuwu, Zhang, Yuehua, Yang, Zhixian
Publicado no Sci Rep (2018)

Phenotype–Genotype Analysis of Chinese Patients with Early-Onset LMNA-Related Muscular Dystrophy

Por Tan, Dandan, Yang, Haipo, Yuan, Yun, Bonnemann, Carsten, Chang, Xingzhi, Wang, Shuang, Wu, Yuchen, Wu, Xiru, Xiong, Hui
Publicado no PLoS One (2015)

Novel copy number variation of POMGNT1 associated with muscle-eye-brain disease detected by next-generation sequencing

Por Fu, Xiaona, Yang, Haipo, Jiao, Hui, Wang, Shuo, Liu, Aijie, Li, Xiaoqing, Xiao, Jiangxi, Yang, Yanling, Wu, Xiru, Xiong, Hui
Publicado no Sci Rep (2017)

Deletion of exon 4 in LAMA2 is the most frequent mutation in Chinese patients with laminin α2-related muscular dystrophy

Por Ge, Lin, Liu, Aijie, Gao, Kai, Du, Renqian, Ding, Juan, Mao, Bing, Hua, Ying, Zhang, Xiaoli, Tan, Dandan, Yang, Haipo, Fu, Xiaona, Fan, Yanbin, Zhang, Ling, Song, Shujuan, Wu, Jian, Zhang, Feng, Jiang, Yuwu, Wu, Xiru, Xiong, Hui
Publicado no Sci Rep (2018)