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  • Molecular assay reagents intended to identify deletions or duplications of the bestrophin 1 (BEST1) gene, located at chromosome 11q13, which encodes the protein bestrophin-1. Genetic variants at this locus have been associated with retinitis pigmentosa 50, autosomal recessive bestrophinopathy, autosomal dominant vitreoretinochoroidopathy, and vitelliform dystrophy.
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