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  • Molecular assay reagents intended to identify genetic variants associated with methylmalonic aciduria with homocystinuria, a genetic disease characterized by deficiencies in vitamin B12 (cobalamin). Genetic variants at multiple loci have been associated with methylmalonic aciduria with homocystinuria. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple methylmalonic aciduria with homocystinuria-associated loci simultaneously.
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