Variants in ST8SIA1 do not play a major role in susceptibility to multiple sclerosis in Canadian families

被引:1
|
作者
Ramagopalan, Sreeram V. [1 ,2 ]
Morrison, Katie M. [1 ,2 ]
Para, Andrea [1 ,2 ]
Handel, Adam [1 ,2 ]
Disanto, Giulio [1 ,2 ]
Handunnetthi, Lahiru [1 ,2 ]
Orton, Sarah M. [1 ,2 ]
Sadovnick, A. Dessa [3 ,4 ]
Ebers, George C. [1 ,2 ]
机构
[1] Wellcome Trust Ctr Human Genet, Oxford, England
[2] Univ Oxford, Dept Clin Neurol, Oxford, England
[3] Univ British Columbia, Dept Med Genet, Vancouver, BC, Canada
[4] Univ British Columbia, Fac Med, Div Neurol, Vancouver, BC, Canada
基金
英国医学研究理事会;
关键词
Multiple sclerosis; Genetics; ST8SIA; POPULATION; LINKAGE; RISK; HAPLOTYPES; ALLELES; DISEASE; COMPLEX; LOCUS;
D O I
10.1016/j.jneuroim.2009.04.017
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Multiple sclerosis (MS) is a complex trait with a significant genetic component. Recent work has implicated the ST8SIA1 gene, encoding a ganglioside synthase, in susceptibility to the disease, perhaps with a parent-of-origin effect. In this investigation of 1318 MS patients from 756 Canadian families, we analysed the transmission of the four single nucleotide polymorphisms in ST8SIA previously shown to be associated with MS. No significant association was found in the entire sample or when stratifying by transmitting parent, indicating that this gene plays little or no role in susceptibility to MS in the Canadian population. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:142 / 144
页数:3
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