Genetic association between EPHX1 and Crohn's disease: population stratification, genotyping error, or random chance?
- PMID: 15306604
- PMCID: PMC1774173
- DOI: 10.1136/gut.2003.032946
Genetic association between EPHX1 and Crohn's disease: population stratification, genotyping error, or random chance?
Comment on
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Genetic polymorphisms in biotransformation enzymes in Crohn's disease: association with microsomal epoxide hydrolase.Gut. 2003 Apr;52(4):547-51. doi: 10.1136/gut.52.4.547. Gut. 2003. PMID: 12631667 Free PMC article.
References
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- Ogura Y , Bonen DK, Inohara N, et al. A frameshift mutation in NOD2 associated with susceptibility to Crohn’s disease. Nature 2001;411:603–6. - PubMed
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- Hugot JP, Chamaillard M, Zouali H, et al. Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn’s disease. Nature 2001;411:599–603. - PubMed
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- Hampe J , Cuthbert A, Croucher PJ, et al. Association between insertion mutation in NOD2 gene and Crohn’s disease in German and British populations. Lancet 2001;357:1925–8. - PubMed
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