Jing Zhang

Gain-of-function mutation of KIT ligand on melanin synthesis causes familial progressive hyperpigmentation.

Xiangyin Kong, Bin Cui, Yu Xia, 2009, American journal of human genetics.

Identification of a novel GPR143 deletion in a Chinese family with X-linked congenital nystagmus

Xiangyin Kong, Landian Hu, Zhiqiang Wang, 2008, Molecular vision.

The mitochondrial transfer RNAAsp A7551G mutation may contribute to the clinical expression of deafness associated with the A1555G mutation in a pedigree with hearing impairment.

Bo Lu, Weiwei Xia, Xiao-Xia Ding, 2018, Molecular medicine reports.