Astroglial glutamate aspartate transporter deficiency

(EAAT2 deficiency)

Synonym(s)
- Early infantile epileptic encephalopathy type 41
Type

Disease
External link(s)
- IEMbase
Gene
- SLC1A2 / Solute Carrier Family 1 Member 2
  11p13
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Glutamate aspartate transporter
Disease group(s)
- 1.11 Disorders of amino acid transport