Top

Published in:

Open Access 01-12-2017 | Correction

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

Authors: Zsolt Bánfai, Kinga Hadzsiev, Endre Pál, Katalin Komlósi, Márton Melegh, László Balikó, Béla Melegh

Published in: BMC Medical Genetics | Issue 1/2017

Excerpt

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. …

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

Title: Correction to: Novel phenotypic variant in the MYH7 spectrum due to a stop-loss mutation in the C-terminal region: a case report
Authors: Zsolt Bánfai
Kinga Hadzsiev
Endre Pál
Katalin Komlósi
Márton Melegh
László Balikó
Béla Melegh
Publication date: 01-12-2017
Publisher: BioMed Central
Published in: BMC Medical Genetics / Issue 1/2017
Electronic ISSN: 1471-2350
DOI: https://doi.org/10.1186/s12881-017-0510-8

At a glance: The STEP trials

Springer Medicine

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

Excerpt

At a glance: The STEP trials

Springer Medicine

Excerpt

Please log in to get access to this content

Other articles of this Issue 1/2017

The three CYBA variants (rs4673, rs1049254 and rs1049255) are benign: new evidence from a patient with CGD

Identification and in silico characterization of a novel p.P208PfsX1 mutation in V-ATPase a3 subunit associated with autosomal recessive osteopetrosis in a Pakistani family

Severe congenital microcephaly with 16p13.11 microdeletion combined with NDE1 mutation, a case report and literature review

ACTA2 mutation and postpartum hemorrhage: a case report

SCN8A mutations in Chinese patients with early onset epileptic encephalopathy and benign infantile seizures

Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sisters