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

Autor Huang, Dan, Zhou, Qiong, Chao, Yun-Qi, Zou, Chao-Chun
Vydáno v Medicine (Baltimore) (2019)

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

Autor Cai, Yu Qing, Zhang, HangHu, Wang, Xiang Zhi, Xu, ChengYun, Chao, Yun Qi, Shu, YingYing, Tang, Lan Fang
Vydáno v Open Forum Infect Dis (2020)