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Molecular assay reagents intended to identify gene variants associated with autosomal recessive forms of retinitis pigmentosa (i.e., forms of retinitis pigmentosa requiring two mutant alleles to be present). Genetic variants at multiple loci have been associated with autosomal recessive 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 recessive retinitis pigmentosa-associated loci simultaneously.
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