Electrophysiological verification of enhanced S-cone syndrome caused by a novel c.755T>C NR2E3 missense variant. (2019)
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/10.1080/13816810.2018.1547912
PubMed Identifier: 30466340
Publication URI: http://europepmc.org/abstract/MED/30466340
Type: Journal Article/Review
Volume: 40
Parent Publication: Ophthalmic genetics
Issue: 1
ISSN: 1381-6810