Dopamine transporter deficiency

Synonym(s)
- Infantile Parkinsonism-dystonia
Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- SLC6A3 / Solute Carrier Family 6 Member 3
  5p15.33
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Dopamine Transporter
Disease group(s)
- 23.1 Monoamine neurotransmission