Identification of novel RHO homozygous mutation in Chinese autosomal recessive retinitis pigmentosa patients.
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DOI: 10.1016/j.exer.2019.107726
Abstract: Retinitis pigmentosa (RP) is a group of genetically heterogeneous retinal diseases with more than 80 identified causative genes to date. The RHO (rhodopsin, OMIM 180380) gene mutation is a hotspot mutation worldwide and is one… read more here.
Keywords: rhodopsin; retinitis pigmentosa; rho homozygous; autosomal recessive ... See more keywords