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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...
Tallennettuna:
| Päätekijät: | , , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2014
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4006458/ https://ncbi.nlm.nih.gov/pubmed/24754962 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1756-8722-7-36 |
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