Ionotropic glutamate receptor NMDA type subunit 2B dysregulation

Synonym(s)
- Early infantile epileptic encephalopathy type 27,
- autosomal dominant intellectual disability type 6
Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- GRIN2B / Glutamate Ionotropic Receptor NMDA Type Subunit 2B
  12p13.1
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Glutamate receptor subunit NR2B
Disease group(s)
- 23.3 Glutamate neurotransmitter disorders