Genetic diagnosis in patients with thrombophilia
Author:
Publisher
Japanese Society on Thrombosis and Hemostasis
Subject
General Medicine
Link
https://www.jstage.jst.go.jp/article/jjsth/26/5/26_518/_pdf
Reference21 articles.
1. 1) Nogami K, Shinozawa K, Ogiwara K, Matsumoto T, Amano K, Fukutake K, Shima M: Novel FV mutation (W1920R, FVNara) associated with serious deep vein thrombosis and more potent APC resistance relative to FVLeiden. Blood 123: 2420–2428, 2014.
2. 2) Miyawaki Y, Suzuki A, Fujita J, Maki A, Okuyama E, Murata M, Takagi A, Murate T, Kunishima S, Sakai M, Okamoto K, Matsushita T, Naoe T, Saito H, Kojima T: Thrombosis from a prothrombin mutation conveying antithrombin resistance. N Engl J Med 366: 2390–2396, 2012.
3. 3) Cooper PC, Goodeve AC, Beauchamp NJ: Quality in molecular biology testing for inherited thrombophilia disorders. Semin Thromb Hemost 38: 600–612, 2012.
4. 4) Kim HJ, Kim DK, Yoo KY, You CW, Yoo JH, Lee KO, Park IA, Choung HS, Kim HJ, Song MJ, Kim SH: Heterogeneous lengths of copy number mutations in human coagulopathy revealed by genome-wide high-density SNP array. Hematologica 97: 304–309, 2012.
5. 5) Sindone AP, Freedman SB: Is risk-benefit of warfarin for atrial fibrillation with heart failure determined by heart failure severity? Thromb Haemost 114: 1–3, 2015.
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