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Disease Info Card
Generalized Progressive Retinal Atrophy
Information about Generalized Progressive Retinal Atrophy: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Generalized Progressive Retinal Atrophy
Most recent studies have shown that Generalized Progressive Retinal Atrophy shares some biological mechanisms with age-related-macular-degeneration, atrophic-retina, atrophy, blind-vision, disorder-of-eye, dog-diseases, dysplasia, dystrophy, hemeralopia, hereditary-diseases, night-blindness, optic-atrophy, retinal-degeneration, retinal-diseases, retinal-dysplasia, retinal-dystrophies, retinitis-pigmentosa.
Among the many pathways, these few ones have gauged particular interests from scientists studying Generalized Progressive Retinal Atrophy, and have been seen in publications frequently: Cell Death, Pathogenesis, Phototransduction, Reflex, Rna Splicing
Quite a number of genes have been found to play important roles in Generalized Progressive Retinal Atrophy, such as ABCA4, ADAM9, ADH7, CACNA2D3, CCDC66, GJD2, ITGB3, LRTM1, MB, MERTK, PDC, PDE6B, PDE6G, PRPH, RCVRN, RNF7, ROM1. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.
Pathways Related to Generalized Progressive Retinal Atrophy
This information is being compiled and will come in a future update
| Cell Death | Pathogenesis | Phototransduction |
| Reflex | Rna Splicing |