Clinical haemochromatosis in HFE mutation carriers
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference4 articles.
1. Penetrance of 845G→A (C282Y) HFE hereditary haemochromatosis mutation in the USA;Beutler;Lancet,2002
2. The effect of HFE mutations on serum ferritin and transferrin saturation in the Jersey population;Merryweather-Clarke;Br J Haematol,1998
3. HFE mutations, iron deficiency and overload in 10,500 blood donors;Jackson;Br J Haematol,2001
4. Dépistage de l'hémochromatose génétique HFE-1 dans une population de diabétiques;Crépin;Ann Endocrinol (Paris),2001
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2. ironXS: high-school screening for hereditary haemochromatosis is acceptable and feasible;European Journal of Human Genetics;2012-01-11
3. Factors influencing disease phenotype and penetrance in HFE haemochromatosis;Human Genetics;2010-07-06
4. The Southern French registry of genetic hemochromatosis: a tool for determining clinical prevalence of the disorder and genotype penetrance;Haematologica;2010-02-09
5. A novel HFE mutation (c.del478) results in nonsense-mediated decay of the mutant transcript in a hemochromatosis patient;Blood Cells, Molecules, and Diseases;2009-09
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