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Prevalence of factor V Leiden and methylenetetrahydrofolate reductase C677T mutations in Azerbaijan.

作者信息

Gurgey A, Rustemov R, Parlak H, Balta G

出版信息

Thromb Haemost. 1998 Sep;80(3):520-1.

PMID:9759638
Abstract
摘要

相似文献

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Prevalence of factor V Leiden and methylenetetrahydrofolate reductase C677T mutations in Azerbaijan.阿塞拜疆因子V莱顿突变和亚甲基四氢叶酸还原酶C677T突变的患病率。
Thromb Haemost. 1998 Sep;80(3):520-1.
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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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Prevalence of prothrombin G20210A, factor V G1691A (Leiden), and methylenetetrahydrofolate reductase (MTHFR) C677T in seven different populations determined by multiplex allele-specific PCR.通过多重等位基因特异性聚合酶链反应测定七个不同人群中凝血酶原G20210A、因子V G1691A(莱顿)和亚甲基四氢叶酸还原酶(MTHFR)C677T的患病率。
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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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A boy with venous thrombosis, homozygous for factor V Leiden, prothrombin G20210A and MTHFR C667t mutations, but belonging to an asymptomatic family.一名患有静脉血栓形成的男孩,为凝血因子V莱顿、凝血酶原G20210A和亚甲基四氢叶酸还原酶C667t突变的纯合子,但来自一个无症状家族。
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[Prevalence of factor V Leiden, hyperhomocysteinemia, prothrombin G20210A, and methylene tetrahydrofolate reductase C677T mutations in obstetrical complications].[产科并发症中因子V莱顿突变、高同型半胱氨酸血症、凝血酶原G20210A突变及亚甲基四氢叶酸还原酶C677T突变的患病率]
Ann Biol Clin (Paris). 1999 Sep-Oct;57(5):539-44.

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Factor V Leiden Mutation Frequency and Geographical Distribution in Turkish Population.土耳其人群中凝血因子V莱顿突变的频率及地理分布
J Transl Int Med. 2020 Dec 31;8(4):268-273. doi: 10.2478/jtim-2020-0040. eCollection 2020 Dec.
2
Postoperative pulmonary embolism in a young female accompanying with Factor V Leiden mutation and hereditary sypherocytosis.
J Thromb Thrombolysis. 2004 Jun;17(3):213-7. doi: 10.1023/B:THRO.0000040491.79092.11.