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Associations of complementation group, ALDH2 genotype, and clonal abnormalities with hematological outcome in Japanese patients with Fanconi anemia

Crossref DOI link: https://doi.org/10.1007/s00277-018-3517-0

Published Online: 2018-10-27

Published Print: 2019-02

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Yabe, Miharu https://orcid.org/0000-0003-0697-5506
Koike, Takashi

Ohtsubo, Keisuke

Imai, Eri

Morimoto, Tsuyoshi

Takakura, Hiromitsu

Koh, Katsuyoshi

Yoshida, Kenichi

Ogawa, Seishi

Ito, Etsuro

Okuno, Yusuke

Muramatsu, Hideki

Kojima, Seiji

Matsuo, Keitaro

Mori, Minako

Hira, Asuka

Takata, Minoru

Yabe, Hiromasa
Funding

Funding for this research was provided by:

Research Grants for Intractable Diseases from the Japanese Ministry of Health, Labor, and Welfare (H21-061)

Research Grants for Intractable Diseases from the Japanese Ministry of Health, Labor, and Welfare (H24-025, H23-012)
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Article History

Received: 28 February 2018

Accepted: 7 October 2018

First Online: 27 October 2018

Compliance with ethical standards

:

: The authors declare that they have no conflict of interest.

: This study was approved by the Research Ethics Committees of Tokai University and Kyoto University, and all procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

: Informed consent was obtained from all individual participants included in the study.