Characterization of two ETFDH mutations in a novel case of riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency.

Name: Characterization of two ETFDH mutations in a novel case of riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency.
Author: Missaglia, Sara

Characterization of two ETFDH mutations in a novel case of riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency. — المؤلف: Missaglia, Sara — Lipids in health and disease 20190129

المؤلف: Missaglia, Sara
النشر: Lipids in health and disease 20190129
الوصف: 254 p.
الموضوعات: Carnitine؛ Computer Simulation؛ DNA Mutational Analysis؛ Drug Therapy, Combination؛ Electron-Transferring Flavoproteins؛ Female؛ Humans؛ Iron-Sulfur Proteins