Mitochondrial coenzyme A transporter deficiency

Type

Disease
External link(s)
- IEMbase
Gene
- SLC25A42 / solute carrier family 25 member 42
  19p13.11
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Mitochondrial carrier protein
Disease group(s)
- 21.5 Disorders of pantothenate and CoA metabolism