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Article

Genotyping for NOD2 genetic variants and crohn disease: a metaanalysis.

Clinical chemistry - 1 Nov 2009

Yazdanyar Shiva, Weischer Maren, Nordestgaard Børge G

Abstract excerpt

BACKGROUND: Arg702Trp, Gly908Arg, and Leu1007fsinsC variants of the NOD2 gene (nucleotide-binding oligomerization domain containing 2; alias, CARD15) influence the risk of Crohn disease. METHODS: We conducted a systematic review to examine whether Arg702Trp, Gly908Arg, and Leu1007fsinsC are equally important risk factors for Crohn disease. In addition, we used studies for which combined information from all...

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Source

Identifiers

PMID: 19713276
DOI: 10.1373/clinchem.2009.127126

Genes

NOD2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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