Rapid progression to AML in a patient with germline GATA2 mutation and acquired NRAS Q61K mutation

GATA2 deficiency syndrome is caused by autosomal dominant, heterozygous germline mutations with widespread effects on immune, pulmonary and vascular systems. Patients commonly develop hematological abnormalities including bone marrow failure, myelodysplastic syndrome (MDS) and acute myeloid leukemia...

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Detalles Bibliográficos
Autores principales: McReynolds, Lisa J., Zhang, Yubo, Yang, Yanqin, Tang, Jingrong, Mulé, Matthew, Hsu, Amy P., Townsley, Danielle M., West, Robert R., Zhu, Jun, Hickstein, Dennis D., Holland, Steven M., Calvo, Katherine R., Hourigan, Christopher S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6582196/
https://www.ncbi.nlm.nih.gov/pubmed/31245276
http://dx.doi.org/10.1016/j.lrr.2019.100176

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6582196/
https://www.ncbi.nlm.nih.gov/pubmed/31245276
http://dx.doi.org/10.1016/j.lrr.2019.100176

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