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Single residue AAV capsid mutation improves transduction of photoreceptors in the Abca4-/- mouse and bipolar cells in the rd1 mouse and human retina ex vivo. (2016)

First Author: De Silva SR
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/10.1038/gt.2016.54

PubMed Identifier: 27416076

Publication URI: http://europepmc.org/abstract/MED/27416076

Type: Journal Article/Review

Volume: 23

Parent Publication: Gene therapy

Issue: 11

ISSN: 0969-7128