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 Mitochondrial dysfunction caused by fatty acids and acylcarnitines Download Scientific Diagram Carnitine: Genetic Variants Affecting Mitochondrial Energy and Health Translating the basic knowledge of mitochondrial functions to metabolic therapy: role of L carnitine ScienceDirect
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l carnitine mitochondrial dysfunction Metabolism: The carnitine shuttle and fatty acid metabolism (practice)