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Prothrombin G20210A Gene Mutation-Induced Recurrent Deep Vein Thrombosis and Pulmonary Embolism: Case Report and Literature Review
Inherited thrombophilia is an important cause of venous thrombosis. The Factor V Leiden (FVL) is the most commonly encountered mutation, followed by the prothrombin G20210A gene mutation (PTM). The typical venous thrombotic events (VTEs) associated with PTM mutations are deep vein thrombosis (DVT) a...
Autores principales: | Elkattawy, Sherif, Alyacoub, Ramez, Singh, Kerry S., Fichadiya, Hardik, Kessler, William |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9016586/ https://www.ncbi.nlm.nih.gov/pubmed/35426321 http://dx.doi.org/10.1177/23247096211058486 |
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