A splice-site variant in FLVCR1 produces retinitis pigmentosa without posterior column ataxia. (2018)
Attributed to:
Developing gene therapy to treat blindness caused by Stargardt Disease
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1080/13816810.2017.1408848
PubMed Identifier: 29192808
Publication URI: http://europepmc.org/abstract/MED/29192808
Type: Journal Article/Review
Volume: 39
Parent Publication: Ophthalmic genetics
Issue: 2
ISSN: 1381-6810