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...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, L., Du, F., Zhang, H.-M., Wang, H.-X.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Associação Brasileira de Divulgação Científica 2015
Materias:
Biomedical Sciences
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

Internet

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

Ejemplares similares