A case report of congenital erythropoietic anemia II in China with a novel mutation

Ann Hematol. 2019 Apr;98(4):1041-1043. doi: 10.1007/s00277-019-03612-2. Epub 2019 Feb 12.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Anemia, Dyserythropoietic, Congenital / genetics*
  • Asian People
  • Child
  • China
  • Female
  • Humans
  • Mutation*
  • Vesicular Transport Proteins / genetics*

Substances

  • SEC23B protein, human
  • Vesicular Transport Proteins