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  • Correction
  • 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

  • 1, 2,
  • 1, 2,
  • 3,
  • 1, 2,
  • ^1, 2,
  • 4 and
  • 1, 2Email author
^Deceased
BMC Medical GeneticsBMC series – open, inclusive and trusted201718:150

https://doi.org/10.1186/s12881-017-0510-8

  • Received: 11 December 2017
  • Accepted: 11 December 2017
  • Published:

The original article was published in BMC Medical Genetics 2017 18:105

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.

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 Medical Genetics, University of Pécs, Szigeti út 12, Pécs, H-7624, Hungary
(2)
Szentágothai Research Centre, University of Pécs, Ifjúság út 20, Pécs, H-7624, Hungary
(3)
Neurology Clinic, University of Pécs, Rét u. 2, Pécs, H-7623, Hungary
(4)
Department of Neurology, Zala County Hospital, Zrínyi u. 1, Zalaegerszeg, H-8900, Hungary

Reference

  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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