Pharmacogenetic typing for oral anti-coagulant response among factor V Leiden mutation carriers

CONTEXT: Factor V Leiden mutation is the most common inherited predisposition for hypercoagulability and thereby a common genetic cause for initiation of oral anti-coagulation therapy. There is a dearth of knowledge of coumarin response profile in such thrombophilic population. AIMS: The current pil...

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Detalles Bibliográficos
Autores principales: Nahar, Risha, Saxena, Renu, Deb, Roumi, Verma, Ishwar C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3656522/
https://www.ncbi.nlm.nih.gov/pubmed/23716941
http://dx.doi.org/10.4103/0971-6866.107987

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3656522/
https://www.ncbi.nlm.nih.gov/pubmed/23716941
http://dx.doi.org/10.4103/0971-6866.107987

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