Detecting genetic variations in hereditary retinal dystrophies with next-generation sequencing technology

por Jin, Xin, Qu, Ling Hui, Meng, Xiao Hong, Xu, Hai Wei, Yin, Zheng Qin
Publicado 2014

Novel mutations in CYP4V2 in Bietti corneoretinal crystalline dystrophy: Next-generation sequencing technology and genotype-phenotype correlations

por Meng, Xiao Hong, He, Yan, Zhao, Tong Tao, Li, Shi Ying, Liu, Yong, Yin, Zheng Qin
Publicado 2019

Novel compound heterozygous mutation in the CNGA1 gene underlie autosomal recessive retinitis pigmentosa in a Chinese family

por Jin, Xin, Qu, Ling-Hui, Hou, Bao-Ke, Xu, Hai-Wei, Meng, Xiao-Hong, Pang, Chi-Pui, Yin, Zheng-Qin
Publicado 2016

Identification of novel CYP4V2 gene mutations in 92 Chinese families with Bietti’s crystalline corneoretinal dystrophy

por Meng, Xiao Hong, Guo, Hong, Xu, Hai Wei, Li, Qi You, Jin, Xin, Bai, Yun, Li, Shi Ying, Yin, Zheng Qin
Publicado 2014

Long-term safety of human retinal progenitor cell transplantation in retinitis pigmentosa patients

por Liu, Yong, Chen, Shao Jun, Li, Shi Ying, Qu, Ling Hui, Meng, Xiao Hong, Wang, Yi, Xu, Hai Wei, Liang, Zhi Qing, Yin, Zheng Qin
Publicado 2017

Identification of 13 novel USH2A mutations in Chinese retinitis pigmentosa and Usher syndrome patients by targeted next-generation sequencing

por Qu, Ling-hui, Jin, Xin, Long, Yan-ling, Ren, Jia-yun, Weng, Chuang-huang, Xu, Hai-wei, Liu, Yong, Meng, Xiao-hong, Li, Shi-ying, Yin, Zheng-qin
Publicado 2020

A phase I clinical trial of human embryonic stem cell‐derived retinal pigment epithelial cells for early‐stage Stargardt macular degeneration: 5‐years' follow‐up

por Li, Shi‐Ying, Liu, Yong, Wang, Lei, Wang, Fang, Zhao, Tong‐Tao, Li, Qi‐You, Xu, Hai‐Wei, Meng, Xiao‐Hong, Hao, Jie, Zhou, Qi, Wang, Liu, Yin, Zheng‐Qin
Publicado 2021