medium chain acyl-CoA-dehydrogenase deficiency(English)
- the most common inherited mitochondrial metabolic disease of fatty acid β-oxidation, typically age 0 to 17 years
- AC, CTD, EMA, FAOD, LCHAD, SCAD, SCADD, VLCADD, DBS, NBS
- Enzymes, Mitochondrion, Pediatrics, Neonatology, Metabolism
- https://doi.org…3023-017-0737-7
- https://doi.org…90/ijms24119657