Examination of the FLT3 and NPM1 mutational status in patients with acute myeloid leukemia from southeastern Poland

INTRODUCTION: Acute myeloid leukemia (AML) is a genetically heterogeneous disease at both the cytogenetic and molecular levels. In AML cells many chromosomal aberrations are observed, some of them being characteristic of a particular subtype of patients, and others being less significant. Besides ch...

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Detalles Bibliográficos
Autores principales: Koczkodaj, Dorota, Zmorzyński, Szymon, Michalak-Wojnowska, Małgorzata, Wąsik-Szczepanek, Ewa, Filip, Agata A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2016
Materias:
Clinical Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4754359/
https://www.ncbi.nlm.nih.gov/pubmed/26925127
http://dx.doi.org/10.5114/aoms.2015.49811

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4754359/
https://www.ncbi.nlm.nih.gov/pubmed/26925127
http://dx.doi.org/10.5114/aoms.2015.49811

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