S-adenosylmethionine carrier deficiency

Synonym(s)
- Combined oxidative phosphorylation deficiency type 28
Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- SLC25A26 / Solute Carrier Family 25 Member 26
  3p14.1
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Mitochondrial carrier protein SLC25A26
Disease group(s)
- 11.1 Disorders of mitochondrial shuttles and carriers