- Open Access
Correction to: Novel phenotypic variant in the MYH7 spectrum due to a stop-loss mutation in the C-terminal region: a case report
- Zsolt Bánfai1, 2,
- Kinga Hadzsiev1, 2,
- Endre Pál3,
- Katalin Komlósi1, 2,
- Márton Melegh^1, 2,
- László Balikó4 and
- Béla Melegh1, 2Email author
© The Author(s). 2017
Received: 11 December 2017
Accepted: 11 December 2017
Published: 16 December 2017
The original article was published in BMC Medical Genetics 2017 18:105
Following publication of the original article , 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.
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.
- 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