Hereditary Hemochromatosis: HFE Mutation Analysis in Greeks Reveals Genetic Heterogeneity

This publication has 14 references indexed in Scilit:

• Commentary on HFE S65C Variant Is Not Associated with Increased Transferrin Saturation in Voluntary Blood Donors by Naveen Arya, Subrata Chakrabrati, Robert A. Hegele, Paul C. Adams
  Blood Cells, Molecules, and Diseases, 1999
• HFE Mutations Analysis in 711 Hemochromatosis Probands: Evidence for S65C Implication in Mild Form of Hemochromatosis
  Blood, 1999
• The Significance of the 187G (H63D) Mutation in Hemochromatosis
  American Journal of Human Genetics, 1997
• Global prevalence of putative haemochromatosis mutations.
  Journal of Medical Genetics, 1997
• 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
• Prevalence of Hemochromatosis among 11,065 Presumably Healthy Blood Donors
  New England Journal of Medicine, 1988
• Juvenile idiopathic haemochromatosis: A life-threatening disorder presenting as hypogonadotropic hypogonadism
  Human Genetics, 1983
• Hereditary Hemochromatosis
  New England Journal of Medicine, 1979
• Association of HLA-A3 and HLA-B14 antigens with idiopathic haemochromatosis.
  Gut, 1976