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Evaluation of a father and son with atypical chronic myeloid leukemia with SETBP1 mutations and a review of the literature
We report the case of a father and son diagnosed with atypical chronic myeloid leukemia (aCML). Both patients harbored SETBP1 mutations, which are present in 24.3% of aCML patients. Moreover, both shared the variant encoding p.Pro737His, but the aCML severity was greater in the son because of the pr...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Associação Brasileira de Divulgação Científica
2015
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4512095/ https://www.ncbi.nlm.nih.gov/pubmed/26017341 http://dx.doi.org/10.1590/1414-431X20154557 |