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Different outcome of six homozygotes for prothrombin A20210A gene variant
Prothrombin G20210A gene variant (FII G20210A) is a risk factor for venous thrombotic disease while conflicting results have been reported for the risk of arterial thrombotic events. However, vascular episodes were absent in up to 40% of the 67 homozygotes for the G20210A described so far, which ind...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2483266/ https://ncbi.nlm.nih.gov/pubmed/18627609 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1479-5876-6-36 |
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