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

Abstract readPublished Erratum

In one paragraph

Article in BMC medical genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it

0cells of the map it votes in

0citing papers in PubMed

–field-weighted citation impact

1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

Erratum for
Novel phenotypic variant in the MYH7 spectrum due to a stop-loss mutation in the C-terminal region: a case report.2017

5 · Who and what money

Authors and funding

7 authors.

Zsolt BánfaiDepartment of Medical Genetics, University of Pécs, Szigeti út 12, Pécs, H-7624, Hungary.

Kinga HadzsievDepartment of Medical Genetics, University of Pécs, Szigeti út 12, Pécs, H-7624, Hungary.

Endre PálNeurology Clinic, University of Pécs, Rét u. 2, Pécs, H-7623, Hungary.

Katalin KomlósiDepartment of Medical Genetics, University of Pécs, Szigeti út 12, Pécs, H-7624, Hungary.

Márton MeleghDepartment of Medical Genetics, University of Pécs, Szigeti út 12, Pécs, H-7624, Hungary.

László BalikóDepartment of Neurology, Zala County Hospital, Zrínyi u. 1, Zalaegerszeg, H-8900, Hungary.

Béla MeleghDepartment of Medical Genetics, University of Pécs, Szigeti út 12, Pécs, H-7624, Hungary. melegh.bela@pte.hu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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

Identifiers

PMID29248012

DOI10.1186/s12881-017-0510-8

PMCPMC5733089

What OpenQuestion holds

Textmetadata

LicenceCC BY

Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.