BMC Medical Genetics (Dec 2017)

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,
Kinga Hadzsiev,
Endre Pál,
Katalin Komlósi,
Márton Melegh,
László Balikó,
Béla Melegh

Affiliations

Zsolt Bánfai: Department of Medical Genetics, University of Pécs
Kinga Hadzsiev: Department of Medical Genetics, University of Pécs
Endre Pál: Neurology Clinic, University of Pécs
Katalin Komlósi: Department of Medical Genetics, University of Pécs
Márton Melegh: Department of Medical Genetics, University of Pécs
László Balikó: Department of Neurology, Zala County Hospital
Béla Melegh: Department of Medical Genetics, University of Pécs

DOI: https://doi.org/10.1186/s12881-017-0510-8
Journal volume & issue: Vol. 18, no. 1
pp. 1 – 1

Abstract

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

Published in BMC Medical Genetics

ISSN: 1471-2350 (Online)
Publisher: BMC
Country of publisher: United Kingdom
LCC subjects: Medicine: Internal medicine; Science: Biology (General): Genetics
Website: https://bmcmedgenet.biomedcentral.com

About the journal