Carnitine: Genetic Variants Affecting Mitochondrial Energy and Health 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 in Mitochondrial Fatty Acid Transport and Oxidation Encyclopedia MDPI Mitochondrial Dysfunction and Chronic Disease DrJockers.com Improving diagnosis of mitochondrial fatty acid oxidation disorders European Journal of Human Genetics Carnitine metabolism in hypertensive heart failure Hypertension Research
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