The significance of the 187G (H63D) mutation in hemochromatosis

Am J Hum Genet. 1997 Sep;61(3):762-4.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.
  • Comment

MeSH terms

  • Gene Frequency
  • HLA Antigens / genetics
  • Hemochromatosis / genetics*
  • Hemochromatosis Protein
  • Heterozygote
  • Histocompatibility Antigens Class I / genetics
  • Homozygote
  • Humans
  • Membrane Proteins*
  • Point Mutation / physiology*

Substances

  • HFE protein, human
  • HLA Antigens
  • Hemochromatosis Protein
  • Histocompatibility Antigens Class I
  • Membrane Proteins