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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)

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Detaylı Bibliyografya
Yayımlandı:Blood
Asıl Yazarlar: Sung, Pamela J., Babushok, Daria V.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: American Society of Hematology 2020
Konular:
Online Erişim: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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