Compound Heterozygotes for Hemochromatosis Gene Mutations: May They Help to Understand the Pathophysiology of the Disease?

This publication has 11 references indexed in Scilit:

• The Hemochromatosis Founder Mutation in HLA-H Disrupts β2-Microglobulin Interaction and Cell Surface Expression
  Journal of Biological Chemistry, 1997
• Commentary
  Blood Cells, Molecules, and Diseases, 1997
• Simple and Rapid Detection of the Newly Described Mutations in the HLA-H Gene
  Blood, 1997
• Genetic irony beyond haemochromatosis: clinical effects of HLA-H mutations
  The Lancet, 1997
• Increased frequency of the haemochromatosis Cys282Tyr mutation in sporadic porphyria cutanea tarda
  The Lancet, 1997
• Clinical and Biochemical Abnormalities in People Heterozygous for Hemochromatosis
  New England Journal of Medicine, 1996
• 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