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Without understanding this distinction, people may assume similar results and safety profiles, leading to uninformed decisions

The essential link between the mitochondrial carnitine transport and FAO is demonstrated by the life-threatening inherited carnitine/acylcarnitine translocase deficiency (OMIM 613698) that, in contrast to the PCD caused by OCTN2 defects, cannot be compensated by the administration of carnitine (Indiveri et al., 2011)