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

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Bibliographic Details
Published inBlood cancer journal (New York) Vol. 6; no. 2; p. e392
Main Authors 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
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 05.02.2016
Nature Publishing Group
Subjects
45
45/22
45/23
631/67/1990/1673
Adult
Alleles
Biomedical and Life Sciences
Biomedicine
Blood Platelet Disorders - complications
Blood Platelet Disorders - diagnosis
Blood Platelet Disorders - genetics
Cancer Research
Cell Transformation, Neoplastic - genetics
Core Binding Factor Alpha 2 Subunit - genetics
Female
Genetic Association Studies
Genetic Predisposition to Disease
Haploinsufficiency
Hematology
Humans
Letter to the Editor
Leukemia, Myeloid, Acute - diagnosis
Leukemia, Myeloid, Acute - etiology
Male
Middle Aged
Oncology
Pedigree
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Bibliography:These authors contributed equally to the work.
ISSN:2044-5385
2044-5385
DOI:10.1038/bcj.2015.81