Evidence map›Paper›PMID 41378130›Full record

ArticleFrontiers in genetics2025

Elise Daire, Elena Panaioli, Cyril Gitiaux, Catherine Gardin, Victor Waldmann, Damien Bonnet, Karim Wahbi, Diala Khraiche

Erratum issuedAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Frontiers in genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Elise DairePediatric Cardiology Department, Amiens University Hospital and Laboratory EA4666 Hematim, University of Picardie-Jules Verne, Amiens, France.
Elena PanaioliM3C-Necker, Congenital and Pediatric Cardiology Department, Necker Enfants malades University Hospital, APHP, Paris, France.
Cyril GitiauxReference Centre for Neuromuscular Diseases, Necker-Enfants malades Hospital, APHP, Paris, France.
Catherine GardinCardiology Departement, Laval Hospital, Laval, France.
Victor WaldmannM3C-Necker, Congenital and Pediatric Cardiology Department, Necker Enfants malades University Hospital, APHP, Paris, France.
Damien BonnetM3C-Necker, Congenital and Pediatric Cardiology Department, Necker Enfants malades University Hospital, APHP, Paris, France.
Karim WahbiUniversity Paris Cité, Paris, France.
Diala KhraicheM3C-Necker, Congenital and Pediatric Cardiology Department, Necker Enfants malades University Hospital, APHP, Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myofibrillar myopathy is a cause of rare and severe pediatric cardiomyopathies. Few descriptions of patients carrying the rare p. Pro209Leu variant in

Indexed as

BAG3Bcl-2-associated athanogene 3cardiomyopathymyofibrillarmyopathypediatricrestrictive cardiomyopathy

Identifiers

PMID41378130
PMCPMC12688876

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.