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A deep vein thrombosis caused by 20209C>T mutation in homozygosis of the prothrombin gene in a Caucasian patient
INTRODUCTION: Additional nucleotide substitutions in the 3′-untranslated region of prothrombin gene could explain some thrombotic events and also adverse pregnancy outcomes. We describe the first case of a homozygous 20209C>T mutation as the cause of deep vein thrombosis in a Spanish patient. CAS...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Croatian Society of Medical Biochemistry and Laboratory Medicine
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3936973/ https://ncbi.nlm.nih.gov/pubmed/24627725 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.11613/BM.2014.018 |
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