Evidence map›Paper›PMID 34441767›Full record

ArticleJournal of clinical medicine2021

Two Novel Variants in

Lidia Carreño-Gago, Diana Luz Juárez-Flores, Josep Maria Grau, Javier Ramón, Ester Lozano, Ferran Vila-Julià, Ramon Martí, Glòria Garrabou, Elena Garcia-Arumí

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 44% of its field
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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Congenital-onset MLASA2 from a novelJournal of neuromuscular diseases · 2026
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Lidia Carreño-GagoResearch Group on Neuromuscular and Mitochondrial Disorders, Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Hospital Universitari, Universitat Autònoma de Barcelona, 08035 Barcelona, Spain.
Diana Luz Juárez-FloresCentro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III, 08036 Barcelona, Spain.
Josep Maria GrauCentro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III, 08036 Barcelona, Spain.
Javier RamónResearch Group on Neuromuscular and Mitochondrial Disorders, Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Hospital Universitari, Universitat Autònoma de Barcelona, 08035 Barcelona, Spain.ORCID 0000-0002-0673-9338
Ester LozanoDepartment of Cell Biology, Physiology and Immunology, University of Barcelona, 08028 Barcelona, Spain.ORCID 0000-0002-6307-9807
Ferran Vila-JuliàResearch Group on Neuromuscular and Mitochondrial Disorders, Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Hospital Universitari, Universitat Autònoma de Barcelona, 08035 Barcelona, Spain.
Ramon MartíResearch Group on Neuromuscular and Mitochondrial Disorders, Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Hospital Universitari, Universitat Autònoma de Barcelona, 08035 Barcelona, Spain.ORCID 0000-0002-8273-9540
Glòria GarrabouCentro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III, 08036 Barcelona, Spain.ORCID 0000-0001-8973-9933
Elena Garcia-ArumíResearch Group on Neuromuscular and Mitochondrial Disorders, Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Hospital Universitari, Universitat Autònoma de Barcelona, 08035 Barcelona, Spain.
Universitat Autònoma de Barcelona · ESInstituto de Salud Carlos III · ESUniversitat de Barcelona · ES

Funding

Instituto de Salud Carlos III PI15/01428Instituto de Salud Carlos III PI18/00498Instituto de Salud Carlos III PI19/01772Instituto de Salud Carlos III PMP15/00025
6 · The paper itself

Abstract

Pathogenic variants in the mitochondrial tyrosyl-tRNA synthetase gene (

Indexed as

mitochondrial aminocyl-tRNA synthetasenovel pathogenic variantPearson’s syndrome

Identifiers

PMID34441767
PMCPMC8397107
OpenAlexW3192691718

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.