Mitochondrial glutamate transporter deficiency

Synonym(s)
- Early infantile epileptic encephalopathy type 3
Type

Disease
External link(s)
- IEMbase
Gene
- SLC25A22 / solute carrier family 25 member 22
  11p15.5
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- mitochondrial glutamate carrier 1
Disease group(s)
- 11.1 Disorders of mitochondrial shuttles and carriers