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Improving diagnosis of mitochondrial fatty acid oxidation disorders European Journal of Human Genetics MCADD (medium chain acyl CoA dehydrogenase deficiency) Disorders of Fatty Acid Metabolism Archives The Medical Biochemistry Page Perioperative management of an adult patient with heterozygous medium chain acyl CoA dehydrogenase deficiency: a case report Cunningham Academic First Place HAC Trine University
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