CDPX

X-linked chondrodysplasia punctata(English)

  • congenital disorder characterized by abnormalities in cartilage and bone development. Mutations leading to amino acid substitutions were identified in the coding region of the arylsulfatase E gene, a novel member of the sulfatase gene family
  • ARSE
  • Congenital disorders
  • https://doi.org/10.1086/301746