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Science 26 February 1988: Vol. 239. no. 4843, pp. 1026 - 1029 DOI: 10.1126/science.2894075
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Articles
Science, Vol 239, Issue 4843, 1026-1029
Copyright © 1988 by American Association for the Advancement of Science
A newly characterized HLA DQ beta allele associated with pemphigus vulgaris
AA Sinha,
C Brautbar,
F Szafer,
A Friedmann,
E Tzfoni,
JA Todd,
L Steinman,
and
HO McDevitt
Department of Medical Microbiology, Stanford University, CA 94305.
The inheritance of particular alleles of major histocompatibility complex class II genes increases the risk for various human autoimmune diseases; however, only a small percentage of individuals having an allele associated with susceptibility develop disease. The identification of allelic variants more precisely correlated with disease susceptibility would greatly facilitate clinical screening and diagnosis. Oligonucleotide-primed gene amplification in vitro was used to determine the nucleotide sequence of a class II variant found almost exclusively in patients with the autoimmune skin disease pemphigus vulgaris. In addition to clinical implications, the disease-restricted distribution of this variant should provide insight into the molecular mechanisms underlying associations between diseases and HLA-class II genes.
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
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- PCR-based HLA class II typing..
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- Pemphigus: An Alternative Approach to Treatment.
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Arch Dermatol
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- Autoimmune diseases: the failure of self tolerance.
- A. Sinha, M. Lopez, and H. McDevitt (1990)
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- Evolution, Function, and Utilization of Major Histocompatibility Complex Polymorphism in Autoimmune Disease.
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- Autoimmune Disease and T-cell Immunologic Recognition.
- L. Hood, V. Kumar, G. Osman, S.S. Beall, C. Gomez, W. Funkhouser, D.H. Kono, D. Nickerson, D.M. Zaller, and J.L. Urban (1989)
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242, 229-237
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- A molecular basis for MHC class II--associated autoimmunity.
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