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; H. Nakajima

doi:10.1038/bcj.2015.81

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, H. Nakajima

Research output: Contribution to journal › Letter › peer-review

18 Citations (Scopus)

Original language	English
Article number	e392
Journal	Blood cancer journal
Volume	6
DOIs	https://doi.org/10.1038/bcj.2015.81
Publication status	Published - 2016 Feb 5

ASJC Scopus subject areas

Hematology
Oncology

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10.1038/bcj.2015.81

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

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

In: Blood cancer journal, Vol. 6, e392, 05.02.2016.

Research output: Contribution to journal › Letter › peer-review

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, vol. 6, e392. https://doi.org/10.1038/bcj.2015.81

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. / Genetic basis of myeloid transformation in familial platelet disorder/acute myeloid leukemia patients with haploinsufficient RUNX1 allele. In: Blood cancer journal. 2016 ; Vol. 6.

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