A New Genetic Disorder in Mitochondrial Fatty Acid β-Oxidation: ACAD9 Deficiency
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics
Reference46 articles.
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3. Purification and properties of rat liver acyl-CoA dehydrogenases and electron transfer flavoprotein;Furuta;J Biochem (Tokyo),1981
4. Human acyl-CoA dehydrogenase-9 plays a novel role in the mitochondrial beta-oxidation of unsaturated fatty acids;Ensenauer;J Biol Chem,2005
5. Cloning and functional characterization of ACAD-9, a novel member of human acyl-CoA dehydrogenase family;Zhang;Biochem Biophys Res Commun,2002
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