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Familial Essential Thrombocythemia With Novel MPL L502G and G208K Mutations
Familial essential thrombocythemia is characterized by the inheritance of germline mutations to progeny, thereby increasing the risk for the development of essential thrombocythemia. Here, we present two cases of young women who developed thromboembolic phenomena, one of whom with an ischemic event ...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Cureus
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9012324/ https://www.ncbi.nlm.nih.gov/pubmed/35449633 http://dx.doi.org/10.7759/cureus.23220 |