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Molecular assay reagents intended to identify gene variants associated with autosomal dominant forms of retinitis pigmentosa (i.e., forms of retinitis pigmentosa requiring only one mutant allele to be present). Genetic variants at multiple loci have been associated with autosomal dominant forms of retinitis pigmentosa. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple autosomal dominant retinitis pigmentosa-associated loci simultaneously.
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