https://www.selleckchem.com/pr....oducts/sodium-bicarb
Gyrate Atrophy (GA) of the choroid and retina (MIM# 25887 is an autosomal recessive disorder due to mutations of the OAT gene encoding ornithine-delta-aminotransferase (OAT), associated with progressive retinal deterioration and blindness. The disease has a theoretical global incidence of approximately 11,500,000. OAT is mainly involved in ornithine catabolism in adults, thus explaining the hyperornithinemia as hallmark of the disease. Patients are treated with an arginine-restricted diet, to limit ornithine load, or the ad
Like
Comment
Share
