Cationic amino acid transporter 2 deficiency

Type

Disease
External link(s)
- IEMbase
Gene
- SLC7A2 / solute carrier family 7 member 2
  8p22
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Amino acid transporter
Disease group(s)
- 1.11 Disorders of amino acid transport