Gene therapy restores vision in rd1 mice after removal of a confounding mutation in Gpr179. (2015)
Attributed to:
Development of an AAV vector for treatment of inherited retinal dystrophy caused by RPE65 deficiency
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1038/ncomms7006
PubMed Identifier: 25613321
Publication URI: http://europepmc.org/abstract/MED/25613321
Type: Journal Article/Review
Volume: 6
Parent Publication: Nature communications
ISSN: 2041-1723