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  • Molecular assay reagents intended to identify gene variants 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 various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple Leber congenital amaurosis-associated loci simultaneously.
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