Genetic basis of myeloid transformation in familial platelet disorder/acute myeloid leukemia patients with haploinsufficient RUNX1 allele

M. Sakurai, H. Kasahara, K. Yoshida, A. Yoshimi, H. Kunimoto, N. Watanabe, Y. Shiraishi, K. Chiba, H. Tanaka, Y. Harada, H. Harada, T. Kawakita, M. Kurokawa, S. Miyano, S. Takahashi, S. Ogawa, S. Okamoto, Hideaki Nakajima

Research output: Contribution to journalLetter

16 Citations (Scopus)
Original languageEnglish
Article numbere392
JournalBlood cancer journal
Volume6
DOIs
Publication statusPublished - 2016 Feb 5

ASJC Scopus subject areas

  • Hematology
  • Oncology

Cite this

Sakurai, M., Kasahara, H., Yoshida, K., Yoshimi, A., Kunimoto, H., Watanabe, N., Shiraishi, Y., Chiba, K., Tanaka, H., Harada, Y., Harada, H., Kawakita, T., Kurokawa, M., Miyano, S., Takahashi, S., Ogawa, S., Okamoto, S., & Nakajima, H. (2016). Genetic basis of myeloid transformation in familial platelet disorder/acute myeloid leukemia patients with haploinsufficient RUNX1 allele. Blood cancer journal, 6, [e392]. https://doi.org/10.1038/bcj.2015.81