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A risk of essential thrombocythemia in carriers of constitutional CHEK2 gene mutations
Germline mutations of the CHEK2 gene have been reported in some myeloid and lymphoid malignancies, but their impact on development of essential thrombocythemia has not been studied. In 16 out of 106 (15.1%) consecutive patients, newly diagnosed with essential thrombocythemia, we found one of four an...
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| Main Authors: | , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Ferrata Storti Foundation
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3291590/ https://ncbi.nlm.nih.gov/pubmed/22058216 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3324/haematol.2011.049494 |
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