A Nonsynonymous SNP in ATG16L1 Predisposes to Ileal Crohn’s Disease and Is Independent of CARD15 and IBD5
Open Access
- 1 May 2007
- journal article
- Published by Elsevier in Gastroenterology
- Vol. 132 (5) , 1665-1671
- https://doi.org/10.1053/j.gastro.2007.03.034
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- Genetics of Crohn disease, an archetypal inflammatory barrier diseaseNature Reviews Genetics, 2005
- Functional variants of OCTN cation transporter genes are associated with Crohn diseaseNature Genetics, 2004
- Genetics of inflammatory bowel disease: progress and prospectsHuman Molecular Genetics, 2004
- The immunological and genetic basis of inflammatory bowel diseaseNature Reviews Immunology, 2003
- Genetic Evidence for Interaction of the 5q31 Cytokine Locus and the CARD15 Gene in Crohn DiseaseAmerican Journal of Human Genetics, 2003
- Inflammatory Bowel DiseaseNew England Journal of Medicine, 2002
- Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn diseaseNature Genetics, 2001
- Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populationsThe Lancet, 2001
- Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's diseaseNature, 2001
- A frameshift mutation in NOD2 associated with susceptibility to Crohn's diseaseNature, 2001