Correction: Habibi I. et al. "Clinical and Genetic Findings of Autosomal Recessive Bestrophinopathy (ARB)" Genes, 2019, , 953.

The authors wish to make a correction to the published version of their paper [...

Clinical and Genetic Findings of Autosomal Recessive Bestrophinopathy (ARB).

Mutations in cause several phenotypes including autosomal dominant (AD) Best vitelliform macular dystrophy type 2 (BVMD), AD vitreo-retino-choroidopathy (ADVIRC), and retinitis pigmentosa-50 (RP50). A rare subtype of Bestrophinopathy exists with biallelic mutations in . Its frequency is estimated to be 1/1,000,000 individuals.