Mitochondrial oxodicarboxylate carrier deficiency

Type

Disease
External link(s)
- IEMbase
Gene
- SLC25A21 / Solute Carrier Family 25 Member 21
  14q13.3
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Mitochondrial carrier protein
Disease group(s)
- 11.1 Disorders of mitochondrial shuttles and carriers