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Article

Association between GRIN3A gene polymorphism in Kawasaki disease and coronary artery aneurysms in Taiwanese children.

PloS one - 1 Jan 2013

Lin Ying-Ju, Chang Jeng-Sheng, Liu Xiang, Hung Chien-Hui, Lin Ting-Hsu, Huang Shao-Mei, Jeang Kuan-Teh, Chen Chia-Yen, Liao Chiu-Chu, Lin Cheng-Wen, Lai Chih-Ho, Tien Ni, Lan Yu-Ching, Ho Mao-Wang, Chien Wen-Kuei, Chen Jin-Hua, Huang Yu-Chuen, Tsang Hsinyi, Wu Jer-Yuarn, Chen Chien-Hsiun, Chang Li-Ching, Tsai Fuu-Jen

Abstract excerpt

Kawasaki disease (KD) is pediatric systemic vasculitis with the classic complication of coronary artery aneurysm (CAA). It is the leading cause of acquired cardiovascular diseases in children. Some severe cases present with multi-organ involvement or neurological dysfunction. To identify the role of the glutamate receptor, ionotropic, N-methyl-d-aspartate 3A (GRIN3A) in KD, we investigated genetic variations in...

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Identifiers

PMID: 24278430
DOI: 10.1371/journal.pone.0081384
PMCID: PMC3838481

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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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