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  • Molecular assay reagents intended to identify the majority of genetic variants known to be associated with porphyria, a collection of genetic diseases caused by deficiencies in heme production. Genetic variants at multiple loci have been associated with porphyria. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in the majority of porphyria-associated loci simultaneously.
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