Kawasaki disease patients homozygous for the rs12252‐C variant of interferon‐induced transmembrane protein‐3 are significantly more likely to develop coronary artery lesions

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Main Authors: Neil E. Bowles, Cammon B. Arrington, Keiichi Hirono, Tsuneyuki Nakamura, Long Ngo, Yin Shen Wee, Fukiko Ichida, John H. Weis
Format: Article
Language:English
Published: Wiley 2014-07-01
Series:Molecular Genetics & Genomic Medicine
Online Access:https://doi.org/10.1002/mgg3.79
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author Neil E. Bowles
Cammon B. Arrington
Keiichi Hirono
Tsuneyuki Nakamura
Long Ngo
Yin Shen Wee
Fukiko Ichida
John H. Weis
author_facet Neil E. Bowles
Cammon B. Arrington
Keiichi Hirono
Tsuneyuki Nakamura
Long Ngo
Yin Shen Wee
Fukiko Ichida
John H. Weis
author_sort Neil E. Bowles
collection DOAJ
format Article
id doaj-art-295ed0ecfa2046649289f892c1a3c0ab
institution OA Journals
issn 2324-9269
language English
publishDate 2014-07-01
publisher Wiley
record_format Article
series Molecular Genetics & Genomic Medicine
spelling doaj-art-295ed0ecfa2046649289f892c1a3c0ab2025-08-20T01:55:12ZengWileyMolecular Genetics & Genomic Medicine2324-92692014-07-012435636110.1002/mgg3.79Kawasaki disease patients homozygous for the rs12252‐C variant of interferon‐induced transmembrane protein‐3 are significantly more likely to develop coronary artery lesionsNeil E. Bowles0Cammon B. Arrington1Keiichi Hirono2Tsuneyuki Nakamura3Long Ngo4Yin Shen Wee5Fukiko Ichida6John H. Weis7Division of Cardiology Department of Pediatrics University of Utah School of Medicine Salt Lake City UtahDivision of Cardiology Department of Pediatrics University of Utah School of Medicine Salt Lake City UtahDepartment of Pediatrics Faculty of Medicine University of Toyama Toyama JapanDepartment of Pediatrics Kanazawa Medical University Kanazawa JapanDepartment of Medicine Harvard Medical School Beth Israel Deaconess Medical Center Brookline MassachusettsDepartment of Pathology University of Utah School of Medicine Salt Lake City UtahDepartment of Pediatrics Faculty of Medicine University of Toyama Toyama JapanDepartment of Pathology University of Utah School of Medicine Salt Lake City Utahhttps://doi.org/10.1002/mgg3.79
spellingShingle Neil E. Bowles
Cammon B. Arrington
Keiichi Hirono
Tsuneyuki Nakamura
Long Ngo
Yin Shen Wee
Fukiko Ichida
John H. Weis
Kawasaki disease patients homozygous for the rs12252‐C variant of interferon‐induced transmembrane protein‐3 are significantly more likely to develop coronary artery lesions
Molecular Genetics & Genomic Medicine
title Kawasaki disease patients homozygous for the rs12252‐C variant of interferon‐induced transmembrane protein‐3 are significantly more likely to develop coronary artery lesions
title_full Kawasaki disease patients homozygous for the rs12252‐C variant of interferon‐induced transmembrane protein‐3 are significantly more likely to develop coronary artery lesions
title_fullStr Kawasaki disease patients homozygous for the rs12252‐C variant of interferon‐induced transmembrane protein‐3 are significantly more likely to develop coronary artery lesions
title_full_unstemmed Kawasaki disease patients homozygous for the rs12252‐C variant of interferon‐induced transmembrane protein‐3 are significantly more likely to develop coronary artery lesions
title_short Kawasaki disease patients homozygous for the rs12252‐C variant of interferon‐induced transmembrane protein‐3 are significantly more likely to develop coronary artery lesions
title_sort kawasaki disease patients homozygous for the rs12252 c variant of interferon induced transmembrane protein 3 are significantly more likely to develop coronary artery lesions
url https://doi.org/10.1002/mgg3.79
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