Expanding the spectrum of A20 haploinsufficiency in two Chinese families: cases report

por Li, Guo-min, Liu, Hai-mei, Guan, Wan-zhen, Xu, Hong, Wu, Bing-bing, Sun, Li
Publicado 2019

Phenotypic variability in a child with Felty’s syndrome: a case report

por Li, Guo-min, Liu, Hai-mei, Guan, Wan-zhen, Li, Yi-fan, Xu, Hong, Sun, Li
Publicado 2020

A mutation in PIK3CD gene causing pediatric systemic lupus erythematosus: A case report

por Li, Guo-Min, Liu, Hai-Mei, Guan, Wan-Zhen, Xu, Hong, Wu, Bing-Bing, Feng, Jia-Yan, Sun, Li
Publicado 2019

A Cohort Study on Deficiency of ADA2 from China

por Li, Guo-min, Han, Xu, Wu, Ye, Wang, Wei, Tang, Hong-xia, Lu, Mei-ping, Tang, Xue-mei, Lin, Yi, Deng, Fan, Yang, Jun, Wang, Xin-ning, Liu, Cong-cong, Zheng, Wen-jie, Wu, Bing-bing, Zhou, Fang, Luo, Hong, Zhang, Liang, Liu, Hai-mei, Guan, Wan-zhen, Wang, Shi-hao, Tao, Pan-feng, Jin, Tai-jie, Fang, Ran, Wu, Yuan, Zhang, Jie, Zhang, Yao, Zhang, Tian-nan, Yin, Wei, Guo, Li, Tang, Wen-jing, Chang, Hong, Zhang, Qiu-ye, Li, Xiao-zhong, Li, Jian-guo, Zhou, Zhi-xuan, Yang, Si-rui, Yang, Kang-kang, Xu, Hong, Song, Hong-mei, Deuitch, Natalie T., Lee, Pui Y., Zhou, Qing, Sun, Li
Publicado 2023