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Prothrombin Gene G20210A Mutation in Acute Deep Venous Thrombosis Patients with Poor Response to Warfarin Therapy

AIM: The pathogenesis of deep venous thrombosis (DVT) involves an interaction between hereditary and acquired factors. Prothrombin gene mutation is one of the hereditary risk factors. We evaluated the frequency of the prothrombin gene mutation in patients with DVT and its relation to oral warfarin a...

詳細記述

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書誌詳細
主要な著者: Attia, F.M, Mikhailidis, D.P, Reffat, S.A
フォーマット: Artigo
言語:Inglês
出版事項: Bentham Open 2009
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC2778014/
https://ncbi.nlm.nih.gov/pubmed/19920886
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2174/1874192400903010147
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