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Born to RUNX1
In this issue of Blood, Simon et al evaluated 430 samples from patients with acute myeloid leukemia (AML) for germline and somatic mutations in RUNX family transcription factor 1 (RUNX1). They found that nearly 30% of the identified variants were germline.(1)
Tallennettuna:
| Julkaisussa: | Blood |
|---|---|
| Päätekijät: | , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
American Society of Hematology
2020
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7243147/ https://ncbi.nlm.nih.gov/pubmed/32437563 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood.2020006152 |
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