Single nucleotide polymorphisms and disease gene mapping

被引：23

作者：

Bell, John I. ^{[1
]}

机构：

[1] John Radcliffe Hosp, Nuffield Dept Clin Med, Oxford OX3 9DU, England

来源：

ARTHRITIS RESEARCH & THERAPY | 2002年 / 4卷 / Suppl 3期

关键词：

disease association; genetics; HLA; linkage disequilibrium; SNP;

D O I：

10.1186/ar555

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Single nucleotide polymorphisms are the most important and basic form of variation in the genome, and they are responsible for genetic effects that produce susceptibility to most autoimmune diseases. The rapid development of databases containing very large numbers of single nucleotide polymorphisms, and the characterization of haplotypes and patterns of linkage disequilibrium throughout the genome, provide a unique opportunity to advance association strategies in common disease rapidly over the next few years. Only the careful use of these strategies and a clear understanding of their statistical limits will allow novel genetic determinants for many of the common autoimmune diseases to be determined.

引用

页码：S273 / S278

页数：6

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