Electron transfer flavoprotein and its role in mitochondrial energy metabolism in health and disease
Author:
Publisher
Elsevier BV
Subject
Genetics,General Medicine
Reference118 articles.
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2. The multiple acyl-coenzyme A dehydrogenation disorders, glutaric aciduria type II and ethylmalonic-adipic aciduria. Mitochondrial fatty acid oxidation, acyl-coenzyme A dehydrogenase, and electron transfer flavoprotein activities in fibroblasts;Amendt;J. Clin. Invest.,1986
3. Assignment of the gene encoding the beta-subunit of the electron-transfer flavoprotein (ETFB) to human chromosome 19q13.3;Antonacci;Genomics,1994
4. Oxidation of the FAD cofactor to the 8-formyl-derivative in human electron-transferring flavoprotein;Augustin;J. Biol. Chem.,2018
5. Short chain acyl-CoA dehydrogenase (ACADS) maps to chromosome 12 (q22-qter) and electron transfer flavoprotein (ETFA) to 15 (q23–q25);Barton;Cytogenet. Cell Genet.,1987
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