Heritable GATA2 mutations associated with familial AML-MDS: a case report and review of literature

A 50-year-old woman was diagnosed with acute myeloid leukemia (AML). She has history of thrombocytopenia for 25 years and a significant family history of thrombocytopenia, affecting her mother, siblings and their children, as well as her own children. Both her mother and maternal aunt died from myel...

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Detalles Bibliográficos
Autores principales: Gao, Juehua, Gentzler, Ryan D, Timms, Andrew E, Horwitz, Marshall S, Frankfurt, Olga, Altman, Jessica K, Peterson, LoAnn C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4006458/
https://www.ncbi.nlm.nih.gov/pubmed/24754962
http://dx.doi.org/10.1186/1756-8722-7-36

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4006458/
https://www.ncbi.nlm.nih.gov/pubmed/24754962
http://dx.doi.org/10.1186/1756-8722-7-36

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