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. 2017 Dec 16;18(1):150. doi: 10.1186/s12881-017-0510-8.

Zsolt Bánfai^{1

2}, Kinga Hadzsiev^{1

2}, Endre Pál³, Katalin Komlósi^{1

2}, Márton Melegh^{1

2}, László Balikó⁴, Béla Melegh^{5

6}

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.
⁵ Department of Medical Genetics, University of Pécs, Szigeti út 12, Pécs, H-7624, Hungary. [email protected].
⁶ Szentágothai Research Centre, University of Pécs, Ifjúság út 20, Pécs, H-7624, Hungary. [email protected].

Abstract

Following publication of the original article [1], the authors requested a correction to the details of one of the co-authors.