Celtic Origin of the C282Y Mutation of Hemochromatosis

This publication has 25 references indexed in Scilit:

• Frequency of the C282Y Mutation of Hemochromatosis in Five French Populations
  Blood Cells, Molecules, and Diseases, 1998
• HFE codon 63/282 (H63D/C282Y) dimorphism in German patients with genetic hemochromatosis
  Tissue Antigens, 1998
• A simple genetic test identifies 90% of UK patients with haemochromatosis
  Gut, 1997
• A High Prevalence of HLA-H 845A Mutations in Hemochromatosis Patients and the Normal Population in Eastern England
  Blood Cells, Molecules, and Diseases, 1997
• Global prevalence of putative haemochromatosis mutations.
  Journal of Medical Genetics, 1997
• Ethnic Differences in the HFE Codon 282 (Cys/Tyr) Polymorphism
  Human Heredity, 1997
• Haemochromatosis and HLA–H
  Nature Genetics, 1996
• Haemochromatosis and HLA–H
  Nature Genetics, 1996
• Mutation Analysis in Hereditary Hemochromatosis
  Blood Cells, Molecules, and Diseases, 1996
• A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosis
  Nature Genetics, 1996