Analysis of Australian Crohn's disease pedigrees refines the localization for susceptibility to inflammatory bowel disease on chromosome 16

被引:85
|
作者
Cavanaugh, JA
Callen, DF
Wilson, SR
Stanford, PM
Sraml, ME
Gorska, M
Crawford, J
Whitmore, SA
Shlegel, C
Foote, S
Kohonen-Corish, AD
Pavli, P
机构
[1] Canberra Hosp, Gastroenterol Unit, Garran, ACT 2606, Australia
[2] Womens & Childrens Hosp, Dept Cytogenet & Mol Genet, Adelaide, SA 5006, Australia
[3] Australian Natl Univ, Ctr Math & Applicat, Canberra, ACT 0200, Australia
[4] Walter & Eliza Hall Inst Med Res, Melbourne, Vic 3050, Australia
[5] Australian Natl Univ, John Curtin Sch Med Res, Div Mol Med, Canberra, ACT 2601, Australia
关键词
D O I
10.1046/j.1469-1809.1998.6240291.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A number of localizations for the putative susceptibility gene(s) have been identified for both Crohn's disease and ulcerative colitis. In a genome wide scan; Hugot et al. (1996) identified a region on chromosome 16 which appeared to be responsible for the inheritance of inflammatory bowel disease in a small proportion of families. Subsequent work has suggested that this localization is important for susceptibility to Crohn's disease rather than ulcerative colitis (Ohmen et al. 1996; Parkes et al. 1996). We investigated the contribution of this localization to the inheritance of inflammatory bowel disease in 54 multiplex Australian families, and confirmed its importance in a significant proportion of Crokn's disease families; we further refined the localization to a region near to D16S409, obtaining a maximum LOD score of 6.3 between D16S409 and D16S753.
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收藏
页码:291 / 298
页数:8
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