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Article

Subcellular localization of mutant P23H rhodopsin in an RFP fusion knockin mouse model of retinitis pigmentosa

2021-10-11

Abstract excerpt

The P23H mutation in rhodopsin (Rho), the visual pigment protein in rod photoreceptor neurons, is the most common genetic cause of autosomal dominant retinitis pigmentosa (adRP), a retinal disease that causes blindness. Despite multiple studies in animal models, the subcellular details of the fate of misfolded mutant Rho in rod photoreceptors have not been completely defined. We generated a new mouse model of adRP...

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Literature Corpus work
cbfaf6f9-13e5-55e1-9417-f45b3e0dcee9
DOI
10.1101/2021.10.11.463949
Open publication

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Subcellular localization of mutant P23H rhodopsin in an RFP fusion knockin mouse model of retinitis pigmentosaDOI 10.1101/2021.10.11.463949
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