Mitochondrial glycine transporter deficiency

Synonym(s)
- Congenital sideroblastic anemia type 2
Type

Disease
External link(s)
- IEMbase
Gene
- SLC25A38 / solute carrier family 25 member 38
  3p22.1
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Mitochondrial carrier protein SLC25A38
Disease group(s)
- 11.1 Disorders of mitochondrial shuttles and carriers