Fat and Sugar Metabolism During Exercise in Patients With Metabolic Myopathy

metabolism, inborn errors, lipid metabolism, inborn errors, carbohydrate metabolism, inborn errors, long-chain 3-hydroxyacyl-coa dehydrogenase deficiency, glycogenin-1 deficiency (glycogen storage disease type xv), carnitine palmitoyl transferase 2 deficiency, vlcad deficiency, medium-chain acyl-coa dehydrogenase deficiency, multiple acyl-coa dehydrogenase deficiency, carnitine transporter deficiency, neutral lipid storage disease, glycogen storage disease type ii