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Article

Prevalence of SLC22A4, SLC22A5 and CARD15 gene mutations in Hungarian pediatric patients with Crohn's disease.

World journal of gastroenterology - 14 Sept 2006

Bene Judit, Magyari Lili, Talián Gábor, Komlósi Katalin, Gasztonyi Beáta, Tari Beáta, Várkonyi Agnes, Mózsik Gyula, Melegh Béla

Abstract excerpt

AIM: To investigate the frequency of the common NOD2/CARD15 susceptibility variants and two functional polymorphisms of OCTN cation transporter genes in Hungarian pediatric patients with Crohn's disease (CD). METHODS: A cohort of 19 unrelated pediatric and 55 unrelated adult patients with Crohn's disease and 49 healthy controls were studied. Genotyping of the three common CD-associated CARD15 variants (Arg702Trp,...

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Identifiers

PMID: 17006998
DOI: 10.3748/wjg.v12.i34.5550
PMCID: PMC4088243

Genes

NOD2

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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