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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Identifiers and source
- Literature Corpus work
- cbfaf6f9-13e5-55e1-9417-f45b3e0dcee9
- DOI
- 10.1101/2021.10.11.463949
