Copper transporter 1 deficiency

Type

Disease
Gene
- SLC31A1 / Solute Carrier Family 31 Member 1
  9q32
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Copper transporter 1
Disease group(s)
- 22.1 Disorders of copper metabolism