医学
亚甲基四氢叶酸还原酶
冠状动脉疾病
疾病
横断面研究
基因多态性
基因
风险因素
内科学
遗传学
基因型
病理
生物
作者
Hairudi Sugijo,Djanggan Sargowo,Edi Widjajanto,Rochmad Romdoni
标识
DOI:10.11604/pamj.2022.41.212.24916
摘要
Introduction: hyperhomocysteinemia (HHcy) may contribute to an increased risk of coronary artery disease (CAD). The underlying mechanisms are not well understood, but other than dietary intake factors, hyperhomocysteinemia may genetically result from a methylenetetrahydrofolate reductase (MTHFR) C677T gene polymorphism. A cross-sectional study was performed to assess whether this mutation was a potential genetic risk factor for CAD.
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