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A common variant of inherited deficiency of type 1A carnitine palmitoyltransferase (CPT1A) first detected in Canadian Inuits has also been detected in the indigenous populations of various regions of Alaska, northern Canada, and Greenland. However, the prevalence of the P479L genotype in neonates has not been evaluated to date. The frequency of the P479L allele in two populations of Taymyr Peninsula...