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[NOD2 gene mutation in Moroccan patients with Crohn's disease: prevalence, genotypic study and correlation of NOD2 gene mutation with the phenotype of Crohn's disease].

The Pan African medical journal - 1 Jan 2017

Tamzaourte Mouna, Errabih Ikram, Krami Hayat, Maha Fadlouallah, Maria Lahmiri, Benzzoubeir Nadia, Ouazzani Laaziza, Sefiani Ahmed, Ouazzani Houria

Abstract excerpt

The aim of this study was to determine the prevalence of NOD2/CARD15 gene mutations in a group of Moroccan patients with Crohn's disease and to study its correlation with genotype-phenotypic expression. We conducted a cross-sectional case-control study over a period of 16 months. 101 patients with Crohn's disease were enrolled between January 2012 and April 2013 as well as a control group of 107 patients. We...

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Identifiers

PMID: 28819537
DOI: 10.11604/pamj.2017.27.116.9187
PMCID: PMC5554695

Genes

NOD2

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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