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Article

NOD2/CARD15 and IL23R genetic variability in 204 Algerian Crohn's disease.

Clinics and research in hepatology and gastroenterology - 1 Sept 2014

Meddour Y, Chaib S, Bousseloub A, Kaddache N, Kecili L, Gamar L, Nakkemouche M, Djidjik R, Abbadi M C, Charron D, Boucekkine T E, Tamouza R

Abstract excerpt

NOD2/CARD15 and IL23R gene variants play an important role in the susceptibility to Crohn's disease (CD). Studies of genotype-phenotype relationship suggest that these variants are associated with the development of the disease and specific phenotype. Preliminary reports analyzing the association between these variants have never been made on Algerian CD's. In a case-control design, 204 Algerian with CD diagnosed...

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Source

Identifiers

PMID: 24679666
DOI: 10.1016/j.clinre.2014.02.003

Genes

NOD2

Variants

rs2066844
rs2066844
rs2066844

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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