Carnitine is an essential cofactor for transport of long chain fatty acids into mitochondria, where oxidation takes place. Carnitine deficiency leads to depressed mitochondrial oxidation of fatty acids, resulting in storage of fat Carnitine: Genetic Variants Affecting Mitochondrial Energy and Health Metabolism of ALCAR in brain. The mitochondrial membrane permeable Download Scientific Diagram Acylcarnitine an overview ScienceDirect Topics
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l carnitine mitochondrial dysfunction Metabolism: The carnitine shuttle and fatty acid metabolism (practice)