Prevalence of the C282Y and H63D mutations in the HFE gene in patients with hereditary haemochromatosis and in control subjects from Northern Germany

Author:

Nielsen ,Carpinteiro ,Fischer ,Cabeda ,Porto ,Gabbe

Publisher

Wiley

Subject

Hematology

Reference11 articles.

1. Mutations in the MHC class I-like candidate gene for hemochromatosis in French patients;Borot;Immunogenetics,1997

2. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis;Feder;Nature Genetics,1996

3. The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding;Feder;Proceedings of the National Academy of Sciences of the United States of America,1998

4. The hemochromatosis founder mutation in HLA-H disrupts β2-microglobulin interaction and cell surface expression;Feder;Journal of Biological Chemistry,1997

5. Fischer , R. Engelhardt , R. Nielsen , P. Gabbe , E.E. Schmiegel , W.H. Wurbs , D. Heinrich , H.C. 1992 Biomagnetism: Clinical Aspects et al 585 588

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