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

被引：0
|
作者：
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
机构：
[1] Keio University School of Medicine,Division of Hematology, Department of Internal Medicine
[2] Graduate School of Medicine,Department of Pathology and Tumor Biology
[3] Kyoto University,Department of Hematology and Oncology
[4] Graduate School of Medicine,Department of Transfusion Medicine & Cell Therapy
[5] The University of Tokyo,Department of Hematology
[6] Keio University School of Medicine,Department of Hematology/Oncology
[7] Laboratory of DNA Information Analysis,undefined
[8] Human Genome Center,undefined
[9] The Institute of Medical Science,undefined
[10] The University of Tokyo,undefined
[11] Laboratory of Sequence Analysis,undefined
[12] Human Genome Center,undefined
[13] The Institute of Medical Science,undefined
[14] The University of Tokyo,undefined
[15] Juntendo University School of Medicine,undefined
[16] The Institute of Medical Science,undefined
[17] The University of Tokyo,undefined
来源：
Blood Cancer Journal | 2016年 / 6卷
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摘要：
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页码：e392 / e392
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