Clinical features and genetic analysis of childhood sitosterolemia: Two case reports and literature review

Por Huang, Dan, Zhou, Qiong, Chao, Yun-Qi, Zou, Chao-Chun
Publicado no Medicine (Baltimore) (2019)

A Novel RFXANK Mutation in a Chinese Child With MHC II Deficiency: Case Report and Literature Review

Por Cai, Yu Qing, Zhang, HangHu, Wang, Xiang Zhi, Xu, ChengYun, Chao, Yun Qi, Shu, YingYing, Tang, Lan Fang
Publicado no Open Forum Infect Dis (2020)