Impaired glutamylation of RPGRORF15 underlies the cone-dominated phenotype associated with truncating distal ORF15 variants. (2022)
Attributed to:
New genetic therapy approaches for inherited retinal diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1073/pnas.2208707119
PubMed Identifier: 36445968
Publication URI: http://europepmc.org/abstract/MED/36445968
Type: Journal Article/Review
Volume: 119
Parent Publication: Proceedings of the National Academy of Sciences of the United States of America
Issue: 49
ISSN: 0027-8424