Results 41 to 50 of about 15,952 (60)
Iron absorption in male C282Y heterozygotes.
Background: The suggestion that carriers of the HFE C282Y mutation absorb nonheme iron more efficiently than do carriers of the wild type has public health implications for countries where the C282Y mutation is common and foods are fortified with iron ...
Jurian Hoogewerff +2 more
exaly +9 more sources
Frequency of the S65C mutation of HFE and iron overload in 309 subjects heterozygous for C282Y
Background/Aims: HFE-related haemochromatosis is a common disorder of iron metabolism. Most affected individuals are homozygous for the C282Y mutation of HFE. Some are compound heterozygotes for C282Y/H63D.
Nathan V Subramaniam +2 more
exaly +2 more sources
Some of the next articles are maybe not open access.
Celtic Origin of the C282Y Mutation of Hemochromatosis
Blood Cells, Molecules, and Diseases, 1998Gérard Lucotte
exaly
Frequency of the C282Y Mutation of Hemochromatosis in Five French Populations
Blood Cells, Molecules, and Diseases, 1998Gérard Lucotte
exaly
Haemochromatosis gene C282Y homozygotes in an elderly male population
Lancet, The, 1999Gavin Willis, I W Fellows, G Willis
exaly
Prevalence of C282Y and H63D mutations in the haemochromatosis (HFE) gene in Tunisian population
Annales De Génétique, 2004Slama Hmida, A Dridi, M Maamar
exaly
Clinical penetrance of C282Y homozygous HFE hemochromatosis
Expert Review of Hematology, 2008John K. Olynyk +2 more
exaly

