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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Detalles Bibliográficos
Autores principales: Attia, F.M, Mikhailidis, D.P, Reffat, S.A
Formato: Texto
Lenguaje:English
Publicado: Bentham Open 2009
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2778014/
https://www.ncbi.nlm.nih.gov/pubmed/19920886
http://dx.doi.org/10.2174/1874192400903010147

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2778014/
https://www.ncbi.nlm.nih.gov/pubmed/19920886
http://dx.doi.org/10.2174/1874192400903010147

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