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Molecular assay reagents intended to identify genetic variants associated with hemochromatosis, a genetic disease characterized by the accumulation of iron in the body. Genetic variants at multiple loci have been associated with hemochromatosis. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple hemochromatosis-associated loci simultaneously.
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