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  • Molecular assay reagents intended to identify gene variants associated with vitreoretinopathy, a hereditary disorder characterized by the failure of blood vessels to form properly at the edges of the retina. Genetic variants at multiple loci have been associated with vitreoretinopathy. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple vitreoretinopathy-associated loci simultaneously.
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