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Monoallelic ABCA4 Mutations Appear Insufficient to Cause Retinopathy: A Quantitative Autofluorescence Study. (2015)

First Author: Müller PL
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