Guang-Hui Jin

Whole‐exome sequencing identified ARL2 as a novel candidate gene for MRCS (microcornea, rod‐cone dystrophy, cataract, and posterior staphyloma) syndrome

Zi-Bing Jin, F. Lu, J. Qu, 2019, Clinical genetics.

Deletion of miR-182 Leads to Retinal Dysfunction in Mice.

Zi-Bing Jin, Lue Xiang, Kun-Chao Wu, 2019, Investigative ophthalmology & visual science.

Whole‐exome sequencing identified ARL2 as a novel candidate gene for MRCS (microcornea, rod‐cone dystrophy, cataract, and posterior staphyloma) syndrome

Zi-Bing Jin, F. Lu, J. Qu, 2018, Clinical genetics.

Ablation of Mature miR-183 Leads to Retinal Dysfunction in Mice

Lue Xiang, Kun-Chao Wu, Xuejiao Chen, 2020, Investigative ophthalmology & visual science.