Clinical haemochromatosis in HFE mutation carriers

Lancet. 2002 Aug 3;360(9330):412-3; author reply 413-4. doi: 10.1016/s0140-6736(02)09583-1.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Blood Donors
  • Female
  • Genetic Markers
  • Health Status*
  • Hemochromatosis / genetics*
  • Hemochromatosis / therapy
  • Homozygote
  • Humans
  • Male
  • Penetrance

Substances

  • Genetic Markers