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  • Molecular assay reagents intended to identify genetic variants associated with maple syrup urine disease, a genetic disease caused by deficiencies in branched-chain amino acid (i.e., isoleucine, leucine, and valine) metabolism. Genetic variants at multiple loci have been associated with maple syrup urine disease. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple maple syrup urine disease-associated loci simultaneously.
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