Gene therapy in the early stages of retinal degeneration
Author:
Funder
NIHR Oxford Biomedical Research Centre
Publisher
Elsevier BV
Reference12 articles.
1. Genetic basis of inherited retinal disease in a molecularly characterized cohort of more than 3000 families from the United Kingdom;Pontikos;Ophthalmology,2020
2. Uber retinitis pigmentosa und angeborene amaurose;Leber;Graefes Arch Clin Exp Ophthalmol,1869
3. Dimerization domain of retinal membrane guanylyl cyclase 1 (RetGC1) is an essential part of guanylyl cyclase-activating protein (GCAP) binding interface;Peshenko;J Biol Chem,2015
4. Regulation of cGMP synthesis in photoreceptors: role in signal transduction and congenital diseases of the retina;Dizhoor;Cell Signal,2000
5. The natural history of Leber congenital amaurosis and cone-rod dystrophy associated with variants in the GUCY2D gene;Hahn;Ophthalmol Retina,2022
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