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Mini-PCDH15 gene therapy rescues hearing in a mouse model of Usher syndrome type 1F | Nature Communications
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Subretinal gene therapy delays vision loss in a Bardet-Biedl Syndrome type 10 mouse model: Molecular Therapy - Nucleic Acids
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CRISPR-Cas9–mediated therapeutic editing of Rpe65 ameliorates the disease phenotypes in a mouse model of Leber congenital amaurosis | Science Advances
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Deficiency of thyroid hormone receptor protects retinal pigment epithelium and photoreceptors from cell death in a mouse model of age-related macular degeneration | Cell Death & Disease
CEP290 gene transfer rescues Leber congenital amaurosis cellular phenotype | Gene Therapy
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In vivo base editing rescues photoreceptors in a mouse model of retinitis pigmentosa: Molecular Therapy - Nucleic Acids
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Natural History of Cone Disease in the Murine Model of Leber Congenital Amaurosis Due to CEP290 Mutation: Determining the Timing and Expectation of Therapy | PLOS ONE
Transcriptional reprogramming restores UBE3A brain-wide and rescues behavioral phenotypes in an Angelman syndrome mouse model - ScienceDirect
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From The Archive: Alexa Chung On Her Lifelong Quest For The Perfect Jeans | British Vogue
NMNAT1 mutations cause Leber congenital amaurosis | Nature Genetics
Frontiers | Exploiting hiPSCs in Leber's Hereditary Optic Neuropathy (LHON): Present Achievements and Future Perspectives
Inhibition of autophagy curtails visual loss in a model of autosomal dominant optic atrophy | Nature Communications
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IJMS | Free Full-Text | Optic Nerve Injury Enhanced Mitochondrial Fission and Increased Mitochondrial Density without Altering the Uniform Mitochondrial Distribution in the Unmyelinated Axons of Retinal Ganglion Cells in a Mouse
In vivo base editing rescues cone photoreceptors in a mouse model of early-onset inherited retinal degeneration | Nature Communications
Caroline Wozniacki: The media needs to move on from Rory and me
Alexa Chung: 'I don't know whether to be open and vulnerable' | Alexa Chung | The Guardian
