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  • Molecular assay reagents intended to identify genetic variants associated with hypermethioninemia, a genetic disorder characterized by deficiencies in methionine metabolism. Genetic variants at multiple loci have been associated with hypermethioninemia. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple hypermethioninemia-associated loci simultaneously.
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