Nature Genetics 37, 1341 - 1344 (2005)
Published online: 13 November 2005; | doi:10.1038/ng1680
Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defectAlienke J Monsuur, Paul I W de Bakker, Behrooz Z Alizadeh, Alexandra Zhernakova, Marianna R Bevova, Eric Strengman, Lude Franke, Ruben van't Slot, Martine J van Belzen, Ineke C M Lavrijsen, Begoña Diosdado, Mark J Daly, Chris J J Mulder, M Luisa Mearin, Jos W R Meijer, Gerrit A Meijer, Erica van Oort, Martin C Wapenaar, Bobby P C Koeleman
& Cisca Wijmenga Supplementary Fig. 1 (pdf 104K)
Study design. Supplementary Fig. 2 (pdf 484K)
Detailed picture of MYO9B and the location of all the SNPs studied in this region. Supplementary Fig. 3 (pdf 476K)
Linkage disequilibrium (LD) plot of the five associated SNPs from the random screen and the one associated SNP from the tag screen showing D' values. Supplementary Fig. 4 (pdf 740K)
Detailed picture of MYO9B and the location of all 35 SNPs currently to be found in HapMap in this region. Supplementary Table 1 (pdf 56K)
Baseline demographics of the cohorts. Supplementary Table 2 (pdf 80K)
Overview of all the random SNPs tested in and around MYO9B, including the details of the tag SNPs used in the comprehensive screen in this region. Supplementary Table 3 (pdf 120K)
Comprehensive screen: statistics of the screen and results of the association study on Set 2 supplemented with cases from Set 1, using tag SNPs. Supplementary Table 4 (pdf 96K)
Sequence analysis of MYO9B.
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