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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...
Gorde:
| Egile Nagusiak: | , , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Medknow Publications & Media Pvt Ltd
2012
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3656522/ https://ncbi.nlm.nih.gov/pubmed/23716941 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0971-6866.107987 |
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