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  • Molecular assay reagents intended to identify deletions or duplications of the carnitine palmitoyltransferase 2 (CPT2) gene, located at chromosome 1p32, which encodes mitochondrial carnitine O-palmitoyltransferase. Genetic variants at this locus have been associated with carnitine palmitoyltransferase II deficiency and susceptibility to infection-induced acute encephalopathy 4.
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