3020insC mutation within the NOD2 gene in Crohn's disease: frequency and association with clinical pattern in an Italian population
- 28 February 2002
- journal article
- other
- Published by Elsevier in Digestive and Liver Disease
- Vol. 34 (2) , 153
- https://doi.org/10.1016/s1590-8658(02)80249-3
Abstract
No abstract availableKeywords
This publication has 3 references indexed in Scilit:
- 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