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Molecular basis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of the major disease-causing mutation in the α-subunit of the mitochondrial trifunctional protein

Mitochondrial BiogenesisBiochemistryMitochondrial FunctionMajor Disease-causing MutationMetabolic DiseaseInherited Metabolic DiseaseGeneticsNatural SciencesMolecular BiologyMetabolic SignalingMitochondrial Trifunctional ProteinMolecular GeneticsMitochondrial BiologyMolecular BasisMetabolismMedicineHuman MetabolismRedox Biology