Corrigendum to "A retrospective study on the clinical and molecular outcomes of calpainopathy in a Turkish patient cohort": [Turkish Journal of Medical Sciences 54 (1) 2024 86-98].

İzem Olcay Şahin, Emine Karataş, Mikail Demir, Büşra Tan, Hüseyin Per, Yusuf Özkul, Munis Dündar

Abstract readPublished Erratum

In one paragraph

Article in Turkish journal of medical sciences, 2024. 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
A retrospective study on the clinical and molecular outcomes of calpainopathy in a Turkish patient cohort.2024

5 · Who and what money

Authors and funding

7 authors.

İzem Olcay ŞahinDepartment of Medical Genetics, Faculty of Medicine, Erciyes University, Kayseri, Turkiye.ORCID https://orcid.org/0000-0002-2105-4767

Emine KarataşDepartment of Medical Genetics, Faculty of Medicine, Erciyes University, Kayseri, Turkiye.ORCID https://orcid.org/0000-0002-8279-8305

Mikail DemirDepartment of Medical Genetics, Faculty of Medicine, Erciyes University, Kayseri, Turkiye.ORCID https://orcid.org/0000-0001-8411-5179

Büşra TanDepartment of Medical Genetics, Faculty of Medicine, Erciyes University, Kayseri, Turkiye.ORCID https://orcid.org/0000-0001-6072-5570

Hüseyin PerDepartment of Pediatric Neurology, Faculty of Medicine, Children's Hospital, Erciyes University, Kayseri, Turkiye.ORCID https://orcid.org/0000-0001-9904-6479

Yusuf ÖzkulDepartment of Medical Genetics, Faculty of Medicine, Erciyes University, Kayseri, Turkiye.ORCID https://orcid.org/0000-0002-4212-5763

Munis DündarDepartment of Medical Genetics, Faculty of Medicine, Erciyes University, Kayseri, Turkiye.ORCID https://orcid.org/0000-0003-0969-4611

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

[This corrects the article DOI: 10.55730/1300-0144.5769.].

Identifiers

PMID39351509

DOI10.55730/1300-0144.5861

PMCPMC11407355

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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.