OnlineIMD

PCYT1A

  • External link(s)
    • 3q29
    • OMIM
    • GnomAD
    • Ensembl
    • HGNC
    • VMH
    • LOVD
  • Associated disease(s)
    • Phosphocholine cytidylyltransferase 1 alpha deficiency, retinoskeletal phenotype