HLA determinants in 70 Danish patients with idiopathic haemochromatosis
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1988.tb03450.x/fullpdf
Reference17 articles.
1. Histocompatibility antigens as markers of abnormal iron metabolism in patients with idiopathic haemochromatosis and their relatives;Bomford;Lancet,1977
2. Hereditary hemochromatosis. Phenotypic expression of the disease;Cartwright;N. Engl. J. Med.,1979
3. Genetic mapping of the hemochromatosis locus on chromosome six;Edwards;Hum. Immunol.,1980
4. Hereditary haemochromatosis;Edwards;Clin. Haematol.,1982
5. HLA determinants in idiopathic hemochromatosis;Fauchet;Tissue Antigens,1979
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1. 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
2. Longer survival associated with HLA-A*03, B*14 among 212 hemochromatosis probands with HFE C282Y homozygosity and HLA-A and -B typing and haplotyping1;European Journal of Haematology;2010-10-21
3. HLA-A, B and DR antigens in patients with gonadal dysgenesis;Clinical Genetics;2008-06-28
4. An HLA study in 74 Danish haemochromatosis patients and in 21 of their families;Clinical Genetics;2008-06-28
5. Human leukocyte antigen haplotypes and HFE mutations in Spanish hereditary hemochromatosis and sporadic porphyria cutanea tarda;Journal of Gastroenterology and Hepatology;2005-03
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