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  • Molecular assay reagents intended to identify mutations in the dihydrolipoamide S-acetyltransferase (DLAT) gene, located at chromosome 11q23.1, which encodes the dihydrolipoyllysine-residue acetyltransferase component of the mitochondrial pyruvate dehydrogenase complex. Genetic variants at this locus have been associated with pyruvate dehydrogenase E2 deficiency.
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