Screening for Wilson’s disease in acute liver failure: A new scoring system in children

por Feng, Cai-Xia, Chen, Xiu-Qi, He, Xiao-Li, Lan, Lian-Cheng, Tang, Qing, Huang, Li, Shan, Qing-Wen
Publicado 2022

Congenital disorder of glycosylation caused by mutation of ATP6AP1 gene (c.1036G>A) in a Chinese infant: A case report

por Yang, Xia, Lv, Zi-Li, Tang, Qing, Chen, Xiu-Qi, Huang, Li, Yang, Mei-Xiong, Lan, Lian-Cheng, Shan, Qing-Wen
Publicado 2021