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Correction to: Novel phenotypic variant in the MYH7 spectrum due to a stop-loss mutation in the C-terminal region: a case report

The Original Article was published on 19 September 2017

Correction

Following publication of the original article [1], the authors requested a correction to the details of one of the co-authors. Professor Béla Melegh had been incorrectly marked by the typesetters with the ^ sign as “deceased” instead of Márton Melegh.

The original article has been updated.

Reference

  1. 1.

    Zsolt Bánfai, Kinga Hadzsiev, Endre Pál, Katalin Komlósi, Márton Melegh, László Balikó and Béla Melegh. BMC Medical Genetics (2017) 18:105 doi: https://doi.org/10.1186/s12881-017-0463-y

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Author notes

  1. Márton Melegh is deceased. This paper is dedicated to his memory.

    • Márton Melegh
  2. The original article can be found online at https://doi.org/10.1186/s12881-017-0463-y.

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    Corresponding author

    Correspondence to Béla Melegh.

    Additional information

    The original article can be found online at https://doi.org/10.1186/s12881-017-0463-y.

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    Open Access This 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.

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    Bánfai, Z., Hadzsiev, K., Pál, E. et al. Correction to: Novel phenotypic variant in the MYH7 spectrum due to a stop-loss mutation in the C-terminal region: a case report. BMC Med Genet 18, 150 (2017). https://doi.org/10.1186/s12881-017-0510-8

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