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Familial essential thrombocythemia: 6 cases from a mono‐institutional series
Rarely essential thrombocythemia (ET) is diagnosed in more than one person within a family. Familial myeloproliferative neoplasms are underdiagnosed. In this report, we describe 6 couples of familial ET, evaluating the heterogeneity of the mutational state and the clinical presentation.
Autores principales: | Accurso, Vincenzo, Santoro, Marco, Mancuso, Salvatrice, Vajana, Giorgia, Tomasello, Riccardo, Rotolo, Cristina, Camarda, Giulia, Mattana, Marta, Siragusa, Sergio |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8886651/ https://www.ncbi.nlm.nih.gov/pubmed/35251652 http://dx.doi.org/10.1002/ccr3.5525 |
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