Novel AAV serotypes for improved ocular gene transfer
Author:
Publisher
Wiley
Subject
Genetics(clinical),Drug Discovery,Genetics,Molecular Biology,Molecular Medicine
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2. Long-Term Restoration of Rod and Cone Vision by Single Dose rAAV-Mediated Gene Transfer to the Retina in a Canine Model of Childhood Blindness
3. In Utero Gene Therapy Rescues Vision in a Murine Model of Congenital Blindness
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