Stationary and Progressive Phenotypes Caused by the p.G90D Mutation in Rhodopsin Gene
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DOI: 10.3390/ijms22042133
Abstract: Mutations in rhodopsin gene (RHO) are a frequent cause of retinitis pigmentosa (RP) and less often, congenital stationary night blindness (CSNB). Mutation p.G90D has previously been associated with CSNB based on the examination of one… read more here.
Keywords: phenotypes caused; stationary progressive; progressive phenotypes; rhodopsin gene ... See more keywords