Mutation analysis of the ATP7B gene and genotype–phenotype correlation in Chinese patients with Wilson disease

by Mingming Li, Jing Ma, Wenlong Wang, Xu Yang, Kaizhong Luo
Published 2021-09-01

Two different pathogenic gene mutations coexisted in the same hereditary spherocytosis family manifested with heterogeneous phenotypes

by Hongwei Shen, Hui Huang, Kaizhong Luo, Yan Yi, Xiaoliu Shi
Published 2019-05-01

HBx down-regulated Gld2 plays a critical role in HBV-related dysregulation of miR-122.

by Feng Peng, Xinqiang Xiao, Yongfang Jiang, Kaizhong Luo, Yi Tian, Milin Peng, Min Zhang, Yun Xu, Guozhong Gong
Published 2014-01-01