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Iron loading and morbidity among relatives of HFE C282Y homozygotes identified either by population genetic testing or presenting as patients

BACKGROUND AND AIMS: Although most cases of hereditary haemochromatosis are associated with homozygosity for the C282Y mutation of the HFE gene, clinical penetrance varies and other genes may modify disease expression. If so, relatives from clinically affected families, by inheriting such genes, may...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
मुख्य लेखकों: McCune, C A, Ravine, D, Carter, K, Jackson, H A, Hutton, D, Hedderich, J, Krawczak, M, Worwood, M
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: BMJ Group 2006
विषय:
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC1856156/
https://ncbi.nlm.nih.gov/pubmed/16174659
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/gut.2005.070342
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