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- W3021571508 abstract "Abstract Retinitis pigmentosa is a retinal degenerative disease that leads to blindness through photoreceptor loss. Rhodopsin is the most frequently mutated protein in this disease. While many rhodopsin mutations have well-understood consequences that lead to cell death, the disease association of several rhodopsin mutations identified in retinitis pigmentosa patients, including F220C and F45L, has been disputed. In this study, we generated two knockin mouse lines bearing each of these mutations. We did not observe any photoreceptor degeneration in either heterozygous or homozygous animals of either line. F220C mice exhibited minor disruptions of photoreceptor outer segment dimensions without any mislocalization of outer segment proteins, whereas photoreceptors of F45L mice were normal. Suction electrode recordings from individual photoreceptors of both mutant lines showed normal flash sensitivity and photoresponse kinetics. Taken together, these data suggest that neither the F220C nor F45L mutation has pathological consequences in mice and, therefore, may not be causative of retinitis pigmentosa in humans." @default.
- W3021571508 created "2020-05-13" @default.
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- W3021571508 date "2020-05-05" @default.
- W3021571508 modified "2023-09-26" @default.
- W3021571508 title "The F220C and F45L rhodopsin mutations identified in retinitis pigmentosa patients do not cause pathology in mice" @default.
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- W3021571508 doi "https://doi.org/10.1038/s41598-020-64437-y" @default.
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