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  • Molecular assay reagents intended to identify deletions or duplications of the dihydrolipoamide branched chain transacylase E2 (DBT) gene, located at chromosome 1p31, which encodes the lipoamide acyltransferase component of the mitochondrial branched-chain alpha-keto acid dehydrogenase complex. Genetic variants at this locus have been associated with maple syrup urine disease.
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