https://www.selleckchem.com/pr....oducts/gsk2795039.ht
er instrument vision screener does not give any recommendation during screening, consider vision- or life-threatening pathology and refer. Autosomal recessive bestrophinopathy (AR is a disease that results from the mutations in the gene. It is characterized by multifocal yellowish lipofuscin deposits, cystoid macular edema, and subretinal fluid. Among approximately 270 mutations, only 40 that include both heterozygous and homozygous mutations are associated with ARB. However, very few ARB-related mutations have been reported in the
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