Associated Papers
HFE gene: Structure, function, mutations, and associated iron abnormalities.
Barton JC et al.
Gene, 2015
The functional significance of E277K and V295A HFE mutations.
Silva B et al.
British Journal of Haematology, 2012
Genetic and metabolic factors are associated with increased hepatic iron stores in a selected population of p.Cys282Tyr heterozygotes.
Mariani R et al.
Blood Cells, Molecules & Diseases, 2010
The molecular genetics of haemochromatosis.
Le Gac G et al.
European Journal of Human Genetics : Ejhg, 2005
The Q283P amino-acid change in HFE leads to structural and functional consequences similar to those described for the mutated 282Y HFE protein.
Ka C et al.
Human Genetics, 2005
[Molecular basis in hereditary haemochromatosis].
Cadet E et al.
La Revue De Medecine Interne, 2005
A previously undescribed nonsense mutation of the HFE gene.
Beutler E et al.
Clinical Genetics, 2002
[Molecular genetics of hemochromatosis].
Rosmorduc O et al.
Journees Annuelles De Diabetologie De L'hotel-dieu, 2002
Differential HFE allele expression in hemochromatosis heterozygotes.
Rosmorduc O et al.
Gastroenterology, 2000
Hematologically important mutations: iron storage diseases.
Beutler L et al.
Blood Cells, Molecules & Diseases, 0
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