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

par Huang, Dan, Zhou, Qiong, Chao, Yun-Qi, Zou, Chao-Chun
Publié dans Medicine (Baltimore) (2019)

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

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