HFE genotypes and haemochromatosis: quantifying the risks of disease
Author:
Publisher
Wiley
Subject
Genetics,Biochemistry,Immunology,General Medicine,Immunology and Allergy
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1399-0039.1999.540310.x/fullpdf
Reference21 articles.
1. Prevalence of hemochromatosis among 11,065 presumably healthy blood donors;Edwards;N Engl J Med,1988
2. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis;Feder;Nat Genet,1996
3. Mutation analysis in hereditary hemochromatosis;Beutler;Blood Cells Mol Dis,1996
4. Haemochromatosis and HLA-H;Jazwinska;Nat Genet,1996
5. Haemochromatosis and HLA-H;Jouanolle;Nat Genet,1996
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1. Simultaneous detection of HFE C282Y, H63D and S65C mutations associated with type 1 haemochromatosis using a multiplex luminex bead assay;Tissue Antigens;2011-07-08
2. Hemochromatosis Genotypes and Risk of Iron Overload—A Meta-Analysis;Annals of Epidemiology;2011-01
3. Hemochromatosis gene mutation—Could it be a disease marker for myelodysplasia?;Leukemia Research;2009-01
4. Psychosocial Impact of Genetic Testing for Hemochromatosis in The HEIRS Study: A Comparison of Participants Recruited in Canada And in The United States;Genetic Testing;2007-04
5. Hemochromatosis (HFE) Gene Mutations and Response to Chloroquine in Porphyria Cutanea Tarda;Archives of Dermatology;2003-03-01
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