Multiple acyl-COA dehydrogenase deficiency in elderly carriers
Francesco Macchione, Leonardo Salviati, Andrea Bordugo, Monica Vincenzi, Marta Camilot, Francesca Teofoli, Elia Pancheri, Roberta Zordan, Cinzia Bertolin, Silvia Rossi, Gaetano Vattemi, Paola Tonin
Topics & Concepts
FlavoproteinNeurologyBeta oxidationMyopathyAcyl CoA dehydrogenaseDifferential diagnosisCarnitineMutationInternal medicineMedicineEndocrinologyGeneDehydrogenaseGeneticsPathologyBiologyBiochemistryEnzymePsychiatryMetabolismMetabolism and Genetic DisordersBiochemical and Molecular ResearchMitochondrial Function and Pathology