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

• Egile Nagusiak: Michael A. Robichaux (Egilea), Vy Nguyen (Egilea), Fung Chan (Egilea), Lavanya Kailasam (Egilea), Feng He (Egilea), John H. Wilson (Egilea), Theodore G. Wensel (Egilea)
• Formatua: Liburua
• Argitaratua: The Company of Biologists, 2022-05-01T00:00:00Z.
• Gaiak: article
• Sarrera elektronikoa: Connect to this object online.

The P23H mutation in rhodopsin (Rho), the rod visual pigment, is the most common allele associated with autosomal-dominant retinitis pigmentosa (adRP). The fate of misfolded mutant Rho in rod photoreceptors has yet to be elucidated. We generated a new mouse model, in which the P23H-Rho mutant allele...