Weining Rong

Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies, rod-cone dystrophies, Leber congenital amaurosis, and cone dysfunction syndromes

Harnessing the potential of hydrogels for advanced therapeutic applications: current achievements and future directions

PRPF4 mutations cause autosomal dominant retinitis pigmentosa

A novel mutation in retinitis pigmentosa GTPase regulator gene with a distinctive retinitis pigmentosa phenotype in a Chinese family.