Mitochondrial β-oxidation of saturated fatty acids in humans

Author:

Adeva-Andany María M.ORCID,Carneiro-Freire Natalia,Seco-Filgueira Mónica,Fernández-Fernández Carlos,Mouriño-Bayolo David

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Molecular Medicine

Reference108 articles.

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3. Short-chain acyl-coenzyme a dehydrogenase deficiency. Clinical and biochemical studies in two patients;Amendt;J. Clin. Invest.,1987

4. A rare disease-associated mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene changes a conserved arginine, previously shown to be functionally essential in short-chain acyl-CoA dehydrogenase (SCAD);Andresen;Am. J. Hum. Genet.,1993

5. Heterogeneous phenotypes in lipid storage myopathy due to ETFDH gene mutations;Angelini,2017

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