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Molecular assay reagents intended to identify gene variants associated with Stargardt disease, a form of macular dystrophy typically characterized by the accumulation of lipofuscin in cells underlying the macula, which leads to progressive central and night vision loss. Genetic variants at multiple loci have been associated with Stargardt disease. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple Stargardt disease-associated loci simultaneously.
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