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Aciduria, Ethylmalonic-Adipic

An autosomal recessive disorder of fatty acid oxidation, and branched chain Amino Acids (Amino Acids, Branched-Chain); Lysine; and Choline catabolism, that is due to defects in either subunit of Electron Transfer Flavoprotein or its Dehydrogenase, Electron Transfer Flavoprotein-Ubiquinone oxidoreductase (EC 1.5.5.1).