Monoallelic ABCA4 Mutations Appear Insufficient to Cause Retinopathy: A Quantitative Autofluorescence Study. (2015)
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/10.1167/iovs.15-17629
PubMed Identifier: 26720470
Publication URI: http://europepmc.org/abstract/MED/26720470
Type: Journal Article/Review
Volume: 56
Parent Publication: Investigative ophthalmology & visual science
Issue: 13
ISSN: 0146-0404