Hypomorphic CDHR1 variants may result in retinitis pigmentosa with relative preservation of cone function. (2024)
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
Volume: 45
Parent Publication: Ophthalmic genetics
Issue: 2
ISSN: 1381-6810