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  • Molecular assay reagents intended to identify mutations in the majority of genes known to be associated with metal accumulation disorders (e.g., iron accumulation [hemochromatosis, ferroportin disease], copper accumulation [Wilson disease]). Genetic variants at multiple loci have been associated with various forms of metal accumulation disorders. These reagents are intended to detect mutations in the majority of the known metal accumulation disorder-associated loci simultaneously.
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