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Article

Pediatric Crohn disease: clinical and genetic characteristics in Taiwan.

Journal of pediatric gastroenterology and nutrition - 1 Mar 2007

Hsiao Cheng-Hui, Wei Shu-Chen, Wong Jau-Min, Lai Hong-Shiee, Chang Mei-Hwei, Ni Yen-Hsuan

Abstract excerpt

OBJECTIVES: Crohn disease (CD) is a heterogeneous disorder. The nucleotide oligomerization domain 2/caspase activating recruitment domain 15 (NOD2/CARD15) gene located at 16q12 is strongly associated with susceptibility to CD in white people but is absent in adult Asian patients, whereas the role of Toll-like receptor 4 (TLR4) polymorphisms has also been reported. Because clinical and genetic data in Asian...

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Source

Identifiers

PMID: 17325555
DOI: 10.1097/MPG.0b013e31802c6997

Genes

NOD2
TLR4

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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