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Article

Involvement of tryptophan hydroxylase 2 (TPH2) gene polymorphisms in susceptibility to coronary artery lesions in Korean children with Kawasaki disease.

European journal of pediatrics - 1 Apr 2010

Park Sung Wook, Ban Ju Yeon, Yoon Kyung Lim, Kim Hak Jae, Chung Jun Young, Yi Jae Woo, Lee Bong Jae, Chung Joo-Ho

Abstract excerpt

Kawasaki disease (KD) is an acute vasculitis of childhood that predominantly affects the coronary arteries. We investigated single nucleotide polymorphisms (SNPs) of the tryptophan hydroxylase 2 (TPH2) gene as risk factors for KD with coronary artery lesions (CALs) in Korean children. We genotyped two SNPs [rs7305115 (exon 7) and rs4290270 (exon 9)] using direct sequencing in 101 KD and 256 control subjects. To...

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Source

Identifiers

PMID: 19763617
DOI: 10.1007/s00431-009-1056-3

Genes

TPH2

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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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