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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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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Attia, F.M, Mikhailidis, D.P, Reffat, S.A
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Bentham Open 2009
Pynciau:
Mynediad Ar-lein: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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