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  • Molecular assay reagents intended to identify deletions and duplications in genes associated with Leber congenital amaurosis, a hereditary retinopathy that leads to vision loss early in life. Genetic variants at multiple loci have been associated with Leber congenital amaurosis. These reagents are intended to detect deletions and duplications in multiple Leber congenital amaurosis-associated loci simultaneously.
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