Additional factor in some HLA DR3/DQ2 haplotypes confers a fourfold increased genetic risk of celiac disease-Reference-Cited by-同舟云学术

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Additional factor in some HLA DR3/DQ2 haplotypes confers a fourfold increased genetic risk of celiac disease

Published:2003-04 Issue:4 Volume:61 Page:308-316
ISSN:0001-2815
Container-title:Tissue Antigens
language:en
Short-container-title:

Author:

Bolognesi E.,Karell K.,Percopo S.,Coto I.,Greco L.,Mantovani V.,Suoraniemi E.,Partanen J.,Mustalahti K.,Mäki M.,Momigliano-Richiardi P.

Publisher

Wiley

Subject

Genetics,Biochemistry,Immunology,General Medicine,Immunology and Allergy

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1399-0039.2003.00028.x/fullpdf

Reference39 articles.

1. Coeliac disease;Maki;Lancet,1997

2. Evidence that celiac disease is primarily associated with a DC locus allelic specificity;Tosi;Clin Immunol Immunopathol,1983

3. Evidence for a primary association of celiac disease to a particular HLA-DQ alpha/beta heterodimer;Sollid;J Exp Med,1989

4. An extended HLA-D region haplotype associated with celiac disease;Howell;Proc Natl Acad Sci USA,1988

5. Celiac patients predominantly inherit HLA-DPB1*0101 positive haplotype from HLA-DQ2 homozygous parent;Polvi;Hum Immunol,1997

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