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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...
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Bentham Open
2009
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| Online Zugang: | 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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