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  • Molecular assay reagents intended to identify deletions or duplications of the carnitine palmitoyltransferase 1A (CPT1A) gene, located at chromosome 11q13.2, which encodes the liver isoform of carnitine O-palmitoyltransferase. Genetic variants at this locus have been associated with carnitine palmitoyltransferase I deficiency.
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