Open Access

Erratum: Heritable GATA2 mutations associated with familial AML-MDS: a case report and review of literature

  • Juehua Gao1Email author,
  • Ryan D. Gentzler2,
  • Andrew E. Timms3, 4,
  • Marshall S. Horwitz3,
  • Olga Frankfurt2,
  • Jessica K. Altman2 and
  • LoAnn C. Peterson1
Journal of Hematology & Oncology20158:131

https://doi.org/10.1186/s13045-015-0228-z

Received: 1 August 2014

Accepted: 21 December 2015

Published: 29 December 2015

The original article was published in Journal of Hematology & Oncology 2014 7:36

After the publication of this work [1], it was brought to our attention that the correct annotation at the protein level for one of the two reported GATA2 mutations is T358N (p.Thr358Asn), but not T358K (p. Thr358Lys), as the forward and reverse sequencing in Fig. 2b were swapped leading to the previous incorrect annotation.

Notes

Declarations

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
Department of Pathology, Northwestern University Feinberg School of Medicine
(2)
Division of Hematology and Oncology, Department of Internal Medicine, Northwestern University Feinberg School of Medicine
(3)
Department of Pathology, University of Washington
(4)
Present address: Seattle Children’s Research Institute

Reference

  1. Gao J, Gentzler RD, Timms AE, Horwitz MS, Frankfurt O, Altman JK, et al. Heritable GATA2 mutations associated with familial AML-MDS: a case report and review of literature. J Hematol Oncol. 2014;7(1):36.PubMedPubMed CentralView ArticleGoogle Scholar

Copyright

© Gao et al. 2015

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