Transferrin receptor 2 mutations in patients with juvenile hemochromatosis phenotype

Am J Hematol. 2015 Dec;90(12):E226-7. doi: 10.1002/ajh.24202. Epub 2015 Nov 17.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Female
  • Hemochromatosis / congenital*
  • Hemochromatosis / genetics
  • Humans
  • Mutation*
  • Phenotype
  • Receptors, Transferrin / genetics*
  • Transfection
  • Young Adult

Substances

  • Receptors, Transferrin

Supplementary concepts

  • Hemochromatosis, type 2