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Article

Association of NOD2/CARD15 mutations on Crohn's disease phenotype in an Italian population.

European journal of gastroenterology & hepatology - 1 Mar 2007

Bianchi Vera, Maconi Giovanni, Ardizzone Sandro, Colombo Elisabetta, Ferrara Elisa, Russo Antonio, Tenchini Maria Luisa, Porro Gabriele Bianchi

Abstract excerpt

AIMS: To confirm the prevalence of NOD2/CARD15 mutations in Italian inflammatory bowel disease patients and to define the role of the different mutations on Crohn's disease phenotype. PATIENTS AND METHODS: A total of 177 patients with Crohn's disease and 92 patients with ulcerative colitis and 164 control participants were investigated for the presence of Arg702Trp, Gly908Arg and Leu1007fsinsC NOD2/CARD15...

Topics

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Colitis, Ulcerative
Crohn Disease
DNA Mutational Analysis
Genetic Predisposition to Disease
Genotype

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Nod2 Signaling Adaptor Protein

Polymorphism, Genetic

Source

Identifiers

PMID: 17301648
DOI: 10.1097/01.meg.0000250590.84102.12

Genes

NOD2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

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