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Evidence for a primary association of celiac disease to a particular HLA-DQ alpha/beta heterodimer.

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Sollid, L M, Markussen, G, Ek, J, Gjerde, H, Vartdal, F, Thorsby, E·1989·The Journal of experimental medicine

Abstract

Typing of DNA from 94 unrelated children with celiac disease (CD) with HLA-DQA1 and -DQB1 allele-specific oligonucleotide probes revealed that all but one (i.e., 98.9%) may share a particular combination of a DQA1 and a DQB1 gene. These genes are arranged in cis position on the DR3DQw2 haplotype and in trans position in DR5DQw7/DR7DQw2 heterozygous individuals. Thus, most CD patients may share the same cis- or trans-encoded HLA-DQ alpha/beta heterodimer.

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Metadata

Authors
Sollid, L. M., Markussen, G., Ek, J., Gjerde, H., Vartdal, F., & Thorsby, E.
Venue
The Journal of experimental medicine
Published
1989-01-01
Volume
169
Issue
1
Pages
345-350
ISSN
  • 0022-1007 (ISSN-L)
  • 1540-9538
OpenAlex
W2048796508
Cited by
931
References
0
FWCI
41.23
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Evidence for a primary association of celiac disease to a particular HLA-DQ alpha/beta heterodimer. https://app.cochat.ai/papers/10.1084/jem.169.1.345
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Sollid, L. M., Markussen, G., Ek, J., Gjerde, H., Vartdal, F., & Thorsby, E. (1989). Evidence for a primary association of celiac disease to a particular HLA-DQ alpha/beta heterodimer. The Journal of experimental medicine. https://doi.org/10.1084/jem.169.1.345

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.