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. 2017 Dec 16;18:150. doi: 10.1186/s12881-017-0510-8

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

Zsolt Bánfai 1,2, Kinga Hadzsiev 1,2, Endre Pál 3, Katalin Komlósi 1,2, Márton Melegh 1,2, László Balikó 4, Béla Melegh 1,2,
PMCID: PMC5733089  PMID: 29248012

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.

Footnotes

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

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

Reference

  • 1.Zsolt Bánfai, Kinga Hadzsiev, Endre Pál, Katalin Komlósi, Márton Melegh, László Balikó and Béla Melegh. BMC Medical Genetics (2017) 18:105 doi: 10.1186/s12881-017-0463-y [DOI] [PMC free article] [PubMed]

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