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Updated: Jan 1, 2026

Limbal Approach-Subretinal Injection of Viral Vectors for Gene Therapy in Mice Retinal Pigment Epithelium
Published on: August 7, 2015
Emerging Concepts for RNA Therapeutics for Inherited Retinal Disease
Spencer M Moore1, Dorota Skowronska-Krawczyk2, Daniel L Chao3
1Medical Scientist Training Program, School of Medicine, University of California, San Diego, La Jolla, CA, USA.
Abstract:
Inherited retinal diseases (IRD) encompass a wide spectrum of hereditary blindness with significant genetic heterogeneity. Therapeutics regulating gene expression on an RNA level have significant promise for treating IRD. In this review, we review the molecular basis of oligonucleotide therapeutics such as ribozymes, RNA interference (RNAi), antisense oligonucleotides (ASO), CRISPRi/a, and their applications to treatments of IRD.
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