Searching for genes influencing a complex disease: the case of coeliac disease

被引:0
|
作者
Åsa Torinsson Naluai
Henry Ascher
Staffan Nilsson
Jan Wahlström
机构
[1] The Sahlgrenska Academy,Department of Genomics
[2] Göteborg University,Department of Clinical Genetics
[3] The Sahlgrenska Academy,Department of Paediatrics
[4] Göteborg University,Department of Mathematical Sciences
[5] The Sahlgrenska Academy,undefined
[6] Göteborg University,undefined
[7] The Nordic School of Public Health,undefined
[8] Chalmers University of Technology,undefined
来源
European Journal of Human Genetics | 2008年 / 16卷
关键词
coeliac (celiac) disease; association; linkage analysis; variation; HLA;
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中图分类号
学科分类号
摘要
Recently, a few genes have been reported to be causative in inflammatory diseases. Still, we are waiting for the vast majority to be discovered. New tools for genotyping and statistical analysis have been developed and emphasis has been put on study design. Coeliac disease (CD) is a disorder, where prolamins in dietary wheat gluten and related proteins from rye or barley are not tolerated. It is one of the most common chronic diseases in humans exceeding a population prevalence of 1%. In this article, we will summarise what is currently known about the genetics influencing CD with the emphasis on the non-HLA genetic component. We will discuss some difficulties when searching for susceptibility genes in disorders with complex inheritance patterns.
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页码:542 / 553
页数:11
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