HFE C282Y homozygotes with serum ferritin concentrations below 1000 μg/L are at low risk of hemochromatosis

HFE-associated hereditary hemochromatosis (HH) is a genetic predisposition to iron overload and subsequent signs and symptoms of disease potentially affecting around 80,000 in Australia and almost one million people in the USA. Most clinical cases are homozygous for the C282Y mutation in the HFE gen...

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Bibliografiset tiedot
Päätekijät: Allen, Katrina J, Bertalli, Nadine A, Osborne, Nicholas J, Constantine, Clare C, Delatycki, Martin B, Nisselle, Amy E, Nicoll, Amanda J, Gertig, Dorota M, McLaren, Christine E, Giles, Graham G, Hopper, John L, Anderson, Gregory J, Olynyk, John K, Powell, Lawrie W, Gurrin, Lyle C
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2010
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2932765/
https://ncbi.nlm.nih.gov/pubmed/20583211
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/hep.23786
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