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Molecular assay reagents intended to identify genetic variants associated with metal accumulation disorders, a collection of genetic diseases caused by deficiencies in metal (e.g., copper, iron) metabolism. Genetic variants at multiple loci have been associated with metal accumulation disorders. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple metal accumulation disorder-associated loci simultaneously.
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