Hypomorphic CDHR1 variants may result in retinitis pigmentosa with relative preservation of cone function. (2023)

First Author: Farag S
Attributed to:  Development of AAV gene therapy for blindness caused by cone-rod dystrophy funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1080/13816810.2023.2255265

PubMed Identifier: 37728066

Publication URI: http://europepmc.org/abstract/MED/37728066

Type: Journal Article/Review

Parent Publication: Ophthalmic genetics

ISSN: 1381-6810