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 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 2020