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The factor V Leiden, prothrombin gene 20210GA, methylenetetrahydrofolate reductase 677CT and platelet glycoprotein IIIa 1565TC mutations in patients with acute ischemic stroke and atrial fibrillation.
Stroke. 2007 Mar;38(3):1069-71. doi: 10.1161/01.STR.0000258076.04860.8e. Epub 2007 Feb 8.
Stroke. 2007.
PMID: 17290027
Hereditary protein C deficiency caused by the Ala267Thr mutation in the protein C gene is associated with symptomatic and asymptomatic venous thrombosis.
Tjeldhorn L, Sandset PM, Haugbro K, Skretting G.
Tjeldhorn L, et al.
Thromb Res. 2010 Mar;125(3):230-4. doi: 10.1016/j.thromres.2009.05.013. Epub 2009 Jun 17.
Thromb Res. 2010.
PMID: 19535131
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Anti-dsDNA antibodies and disease classification in antinuclear antibody positive patients: the role of analytical diversity.
Haugbro K, Nossent JC, Winkler T, Figenschau Y, Rekvig OP.
Haugbro K, et al.
Ann Rheum Dis. 2004 Apr;63(4):386-94. doi: 10.1136/ard.2003.016303.
Ann Rheum Dis. 2004.
PMID: 15020332
Free PMC article.
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