Phenylalanine Hydroxylase Deficiency and Citrin Deficiency in a Chinese Infant

por Ye, Jun, Qiu, Wen-Juan, Han, Lian-Shu, Zhang, Hui-Wen, Gu, Xue-Fan
Publicado no Chin Med J (Engl) (2015)

Elevated Bile Acids in Newborns with Biliary Atresia (BA)

por Zhou, Kejun, Lin, Na, Xiao, Yongtao, Wang, Yang, Wen, Jie, Zou, Gang-Ming, Gu, XueFan, Cai, Wei
Publicado em 2012

Identification of predominant GNPTAB gene mutations in Eastern Chinese patients with mucolipidosis II/III and a prenatal diagnosis of mucolipidosis II

por Wang, Yu, Ye, Jun, Qiu, Wen-juan, Han, Lian-shu, Gao, Xiao-lan, Liang, Li-li, Gu, Xue-fan, Zhang, Hui-wen
Publicado no Acta Pharmacol Sin (2018)

Correlation of ATP7B genotype with phenotype in Chinese patients with Wilson disease

por Liu, Xiao-Qing, Zhang, Ya-Fen, Liu, Tze-Tze, Hsiao, Kwang-Jen, Zhang, Jian-Ming, Gu, Xue-Fan, Bao, Ke-Rong, Yu, Li-Hua, Wang, Mei-Xian
Publicado no World J Gastroenterol (2004)