The HLA-A1-B8 haplotype hitchhiking with the hemochromatosis mutation: does it affect the phenotype?
Author:
Publisher
Wiley
Subject
Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.2007.00953.x/fullpdf
Reference36 articles.
1. A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosis
2. Hereditary Hemochromatosis — A New Look at an Old Disease
3. Penetrance of 845G→A (C282Y) HFE hereditary haemochromatosis mutation in the USA
4. Hemochromatosis and Iron-Overload Screening in a Racially Diverse Population
5. The ancestral hemochromatosis haplotype is associated with a severe phenotype expression in Italian patients
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1. The ancestral haplotype markers HLA -A3 and B7 do not influence the likelihood of advanced hepatic fibrosis or cirrhosis in HFE hemochromatosis;Scientific Reports;2023-05-13
2. Iron loading in HFE p.C282Y homozygotes found by population screening: relationships to HLA-type and T-lymphocyte subsets;Scandinavian Journal of Clinical and Laboratory Investigation;2017-07-05
3. Synthesis and evaluation of a novel rhodamine B-based ‘off-on’ fluorescent chemosensor for the selective determination of Fe3+ ions;Sensors and Actuators B: Chemical;2017-04
4. White blood cells and subtypes in HFE p.C282Y and wild-type homozygotes in the Hemochromatosis and Iron Overload Screening Study;Blood Cells, Molecules, and Diseases;2017-03
5. Autoimmune Conditions in 235 Hemochromatosis Probands withHFEC282Y Homozygosity and Their First-Degree Relatives;Journal of Immunology Research;2015
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