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P225 - Association between NOD2, ATG16L1 And IL23R gene polymorphisms and childhood-onset of Crohn's disease: results from a case control study among Greek cases

✍ Scribed by M. Gazouli; I. Pachoula; I. Panayotou; G.J. Mantzaris; A. Franke; G. Chroussos; S. Schreiber; N. Anagnou; E. Roma-Giannikou


Book ID
119636340
Publisher
Oxford University Press
Year
2009
Tongue
English
Weight
50 KB
Volume
3
Category
Article
ISSN
1873-9946

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Contributions of IBD5, IL23R, ATG16L1, a
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Background: IBD5, IL23R, and ATG16L1 genetic variations are established Crohn's disease (CD) risks alleles. We evaluated these in a population-based case-control study within a cohort to determine their penetrance, population attributable risk, independence, and relationship to other established CD