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The mutation C677T in the methylene tetrahydrofolate reductase gene as a risk factor for myocardial infarction in the Portuguese population.

作者信息

Ferrer-Antunes C, Palmeiro A, Morais J, Lourenço M, Freitas M, Providência L

出版信息

Thromb Haemost. 1998 Sep;80(3):521-2.

PMID:9759639
Abstract
摘要

相似文献

1
The mutation C677T in the methylene tetrahydrofolate reductase gene as a risk factor for myocardial infarction in the Portuguese population.亚甲基四氢叶酸还原酶基因中的C677T突变作为葡萄牙人群中心肌梗死的一个危险因素。
Thromb Haemost. 1998 Sep;80(3):521-2.
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Factor V G1691A, apo E4 allele, hyperhomocysteinemia and MTHFR C677T in a young patient with myocardial infarction.
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C677T substitution in the methylenetetrahydrofolate reductase gene as a risk factor for venous thrombosis and arterial disease in selected patients.亚甲基四氢叶酸还原酶基因中的C677T替换作为特定患者静脉血栓形成和动脉疾病的危险因素。
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Hyperhomocysteinemia, MTHFR C677T genotype and low folate levels: a risk combination for acute coronary disease in a Portuguese population.
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The mutation C677-->T in the methylene tetrahydrofolate reductase gene and stroke.
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Genetic polymorphism of 5,10-MTHFR reductase gene in offspring of patients with myocardial infarction.心肌梗死患者后代中5,10-亚甲基四氢叶酸还原酶基因的遗传多态性
Thromb Haemost. 1999 Jul;82(1):19-23.
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Genetic coronary risk factors in conventionally low-risk patients.传统低风险患者中的遗传性冠状动脉危险因素。
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The C677T mutation in the methylene tetrahydrofolate reductase gene increases serum uric acid in elderly men.亚甲基四氢叶酸还原酶基因中的C677T突变会使老年男性的血清尿酸升高。
J Hum Genet. 2000;45(4):257-62. doi: 10.1007/s100380070037.
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Prevalence of the methylenetetrahydrofolate reductase (MTHFR) C677T mutation in patients with varicose veins of lower limbs.下肢静脉曲张患者亚甲基四氢叶酸还原酶(MTHFR)C677T突变的患病率
Mol Genet Metab. 1998 Jan;63(1):35-6. doi: 10.1006/mgme.1997.2638.
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High frequency of the C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene in Northern Italy.意大利北部亚甲基四氢叶酸还原酶(MTHFR)基因中C677T突变的高频率。
Thromb Haemost. 1997 Aug;78(2):963-4.

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gene polymorphisms and susceptibility to myocardial infarction: Evidence from meta-analysis and trial sequential analysis.基因多态性与心肌梗死易感性:来自荟萃分析和试验序贯分析的证据。
Int J Cardiol Heart Vasc. 2023 Nov 22;49:101293. doi: 10.1016/j.ijcha.2023.101293. eCollection 2023 Dec.
2
Candidate genes and confirmed genetic polymorphisms associated with cardiovascular diseases: a tabular assessment.与心血管疾病相关的候选基因和已证实的基因多态性:表格评估
J Thromb Thrombolysis. 2001 Feb;11(1):49-81. doi: 10.1023/a:1008956327032.