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Clinical implications of subclonal TP53 mutations in acute myeloid leukemia
The role of subclonal TP53 mutations, defined by a variant allele frequency of <20%, has not been addressed in acute myeloid leukemia yet. We, therefore, analyzed their prognostic value in a cohort of 1,537 patients with newly diagnosed disease, prospectively treated within three trials of the “G...
Kaydedildi:
| Yayımlandı: | Haematologica |
|---|---|
| Asıl Yazarlar: | , , , , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Ferrata Storti Foundation
2019
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6395341/ https://ncbi.nlm.nih.gov/pubmed/30309854 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3324/haematol.2018.205013 |
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