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)
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