A Novel MIP Gene Mutation Analysis in a Chinese Family Affected with Congenital Progressive Punctate Cataract

por Ding, Xuchen, Zhou, Nan, Lin, Hui, Chen, Jianjun, Zhao, Chunyuan, Zhou, Guangkai, Hejtmancik, J. Fielding, Qi, Yanhua
Publicado 2014

Genetic analysis of the FOXL2 gene using quantitative real-time PCR in Chinese patients with blepharophimosis-ptosis-epicanthus inversus syndrome

por Hu, Shanshan, Guo, Junjing, Wang, Binbin, Wang, Jing, Zhou, Zhou, Zhou, Guangkai, Ding, Xuchen, Ma, Xu, Qi, Yanhua
Publicado 2011

A novel mutation in the connexin 46 (GJA3) gene associated with congenital cataract in a Chinese pedigree

por Ding, Xuchen, Wang, Binbin, Luo, Yongfeng, Hu, Shanshan, Zhou, Guangkai, Zhou, Zhou, Wang, Jing, Ma, Xu, Qi, Yanhua
Publicado 2011