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  • Molecular assay reagents intended to identify mutations in the carnitine palmitoyltransferase II (CPT2) gene, located at chromosome 1p32, which encodes for carnitine palmitoyltransferase II that participates in transporting long-chain fatty acids into the mitochondria. Mutations at this locus have been identified in patients with carnitine palmitoyltransferase II (CPT2) deficiency.
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