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Blood Cancer J. 2016 Feb 5;6:e392. doi: 10.1038/bcj.2015.81.

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

Author information

1
Division of Hematology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan.
2
Department of Pathology and Tumor Biology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
3
Department of Hematology and Oncology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
4
Department of Transfusion Medicine & Cell Therapy, Keio University School of Medicine, Tokyo, Japan.
5
Laboratory of DNA Information Analysis, Human Genome Center, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
6
Laboratory of Sequence Analysis, Human Genome Center, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
7
Department of Hematology, Juntendo University School of Medicine, Tokyo, Japan.
8
Department of Hematology/Oncology, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
PMID:
26849013
PMCID:
PMC4771963
DOI:
10.1038/bcj.2015.81
[Indexed for MEDLINE]
Free PMC Article

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