An (192)Arg variant of the human paraoxonase (HUMPONA) gene polymorphisms is associated for with the increased risk for coronary artery disease in the Japanese

被引：0
|
作者：
Zama, T
Murata, M
Matsubara, Y
Kawano, K
Aoki, N
Yoshino, H
Watanabe, G
Ishikawa, K
Ikeda, Y
机构：
[1] KEIO UNIV, SCH MED, DEPT MED, TOKYO 160, JAPAN
[2] KYORIN UNIV, DEPT MED 2, TOKYO, JAPAN
[3] HIBIYA MED CTR, SAKURA BANK, TOKYO, JAPAN
来源：
THROMBOSIS AND HAEMOSTASIS | 1997年
关键词：
D O I：
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中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
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页码：P2129 / P2129
页数：1
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  • [3] The Gln-Arg191 polymorphism of the human paraoxonase gene (HUMPONA) is not associated with the risk of coronary artery disease in Finns
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  • [4] The methionine variant at codon 55, but not the GLN192ARG polymorphism of the human paraoxonase gene is associated with coronary artery disease
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  • [5] The gln-arg192 polymorphism of human paraoxonase gene is not associated with coronary artery disease in Italian patients
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