A Specific Macula-Predominant Retinal Phenotype Is Associated With the CDHR1 Variant c.783G>A, a Silent Mutation Leading to In-Frame Exon Skipping. (2019)

First Author: Charbel Issa P
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/10.1167/iovs.18-26415

PubMed Identifier: 31387115

Publication URI: http://europepmc.org/abstract/MED/31387115

Type: Journal Article/Review

Volume: 60

Parent Publication: Investigative ophthalmology & visual science

Issue: 10

ISSN: 0146-0404