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Tropism of engineered and evolved recombinant AAV serotypes in the rd1 mouse and ex vivo primate retina. (2017)

First Author: Hickey DG
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.2017.85

PubMed Identifier: 28872643

Publication URI: http://europepmc.org/abstract/MED/28872643

Type: Journal Article/Review

Volume: 24

Parent Publication: Gene therapy

Issue: 12

ISSN: 0969-7128