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Prevalence of the methylenetetrahydrofolate reductase (MTHFR) C677T mutation in patients with varicose veins of lower limbs.

作者信息

Sverdlova A M, Bubnova N A, Baranovskaya S S, Vasina V I, Avitisjan A O, Schwartz E I

出版信息

Mol Genet Metab. 1998 Jan;63(1):35-6. doi: 10.1006/mgme.1997.2638.

DOI:10.1006/mgme.1997.2638
PMID:9538515
Abstract
摘要

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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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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 and the MTHFR C677T mutation in Budd-Chiari syndrome.布加综合征中的高同型半胱氨酸血症与亚甲基四氢叶酸还原酶C677T突变
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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。
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Methylenetetrahydrofolate reductase gene polymorphism as a risk factor for diabetic nephropathy in IDDM patients.亚甲基四氢叶酸还原酶基因多态性作为胰岛素依赖型糖尿病患者糖尿病肾病的危险因素
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Effects of factor V gene G1691A, methylenetetrahydrofolate reductase gene C677T, and prothombin gene G20210A mutations on deep venous thrombogenesis in Behçet's disease.因子V基因G1691A、亚甲基四氢叶酸还原酶基因C677T和凝血酶原基因G20210A突变对白塞病深静脉血栓形成的影响。
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[C677T genetic polymorphism of methylenetetrahydrofolate reductase in premature coronary heart disease].亚甲基四氢叶酸还原酶C677T基因多态性与早发冠心病
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The methylentetrahydrofolate reductase C677T point mutation is a risk factor for vascular access thrombosis in hemodialysis patients.亚甲基四氢叶酸还原酶C677T点突变是血液透析患者血管通路血栓形成的一个危险因素。
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Is there a role for genetic polymorphism of C677T methylenetetrahydrofolate reductase (MTHFR) in Buerger's disease?
Thromb Haemost. 2000 Oct;84(4):736-7.

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