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Disease Info Card
Leber Congenital Amaurosis
Information about Leber Congenital Amaurosis: 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 Leber Congenital Amaurosis
Most recent studies have shown that Leber Congenital Amaurosis shares some biological mechanisms with abnormal-degeneration, age-related-macular-degeneration, amaurosis, atrophy, blind-vision, blindness-congenital, dystrophy, kidney-diseases, night-blindness, nystagmus, optic-atrophies-hereditary, optic-atrophy-hereditary-leber, retinal-degeneration, retinal-diseases, retinal-dystrophies, retinitis-pigmentosa, visual-impairment.
Among the many pathways, these few ones have gauged particular interests from scientists studying Leber Congenital Amaurosis, and have been seen in publications frequently: Cell Adhesion, Cell Cycle, Cell Death, Gene Silencing, Hatching, Immune Response, Localization, Nuclear Transport, Pathogenesis, Phototransduction, Pigmentation, Programmed Cell Death, Protein Folding, Reflex, Regeneration, Secretion, Translation, Transport, Tropism, Visual Behavior
Quite a number of genes have been found to play important roles in Leber Congenital Amaurosis, such as AIPL1, CEP290, CLTA, CRB1, CRX, ERG, GUCA1A, GUCY2D, KCNH2, LCA5, LRAT, PTPRC, RDH12, RHO, RPE, RPE65, RPGR, RPGRIP1. 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.