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Article

CARD15 mutations are rare in Swedish pediatric Crohn disease.

Journal of pediatric gastroenterology and nutrition - 1 Apr 2005

Ideström Maja, Rubio Carlos, Granath Fredrik, Finkel Yigael, Hugot J-P

Abstract excerpt

BACKGROUND: An association between mutations in a gene involved in bacterial recognition by monocytes, CARD15/NOD2 and Crohn disease (CD) has been reported in studies of adults and children. The aim of this study was to investigate the presence of CARD15 mutations in Swedish children with CD and analyze genotype-phenotype correlations. PATIENTS AND METHODS: Fifty-eight children (62% boys) with CD diagnosed...

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Source

Identifiers

PMID: 15795594
DOI: 10.1097/01.mpg.0000150423.38210.2e

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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