Norepinephrine transporter deficiency

Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- SLC6A2 / Solute Carrier Family 6 Member 2
  16q12.2
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Norepinephrine transporter
Disease group(s)
- 23.1 Monoamine neurotransmission