Vesicular monoamine transporter 2 deficiency

Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- SLC18A2 / Solute Carrier Family 18 Member A2
  10q25.3
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Vesicular monoamine transporter 2
Disease group(s)
- 23.1 Monoamine neurotransmission