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  • Molecular assay reagents intended to identify deletions and duplications in genes 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 deletions and duplications in multiple methylmalonic aciduria with homocystinuria-associated loci simultaneously.
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