Reply to “Rare coincident NPM1 and RUNX1 mutations in intermediate risk acute myeloid leukemia display similar patterns to single mutated cases”. Haematologica 2014;99(2):e20–21.
oleh: Jason H. Mendler, Guido Marcucci, Clara D. Bloomfield
| Format: | Article |
|---|---|
| Diterbitkan: | Ferrata Storti Foundation 2014-02-01 |
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