Evidence map›Paper›PMID 33850219›Full record

ArticleScientific reports2021

Author Correction: Epilepsy and neuropsychiatric comorbidities in mice carrying a recurrent Dravet syndrome SCN1A missense mutation.

Ana Ricobaraza, Lucia Mora-Jimenez, Elena Puerta, Rocio Sanchez-Carpintero, Ana Mingorance, Julio Artieda, Maria Jesus Nicolas, Guillermo Besne, Maria Bunuales, Manuela Gonzalez-Aparicio and 3 more

Open access · goldAbstract readPublished Erratum
In one paragraph

Article in Scientific reports, 2021. 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, top 96% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 1 country.

Ana RicobarazaGene Therapy Program CIMA, IdiSNA, Navarra institute for health research, University of Navarra, Pamplona, Spain. aricobaraza@unav.es.ORCID http://orcid.org/0000-0001-7587-7657
Lucia Mora-JimenezGene Therapy Program CIMA, IdiSNA, Navarra institute for health research, University of Navarra, Pamplona, Spain.
Elena PuertaDepartment of Pharmacology and Toxicology, IdiSNA, Navarra institute for health research, University of Navarra, Pamplona, Spain.
Rocio Sanchez-CarpinteroDravet Syndrome Unit, Pediatric Neurology Unit, IdiSNA, Navarra institute for health research, University Clinic of Navarra, Pamplona, Spain.
Ana MingoranceDracaena Consulting, Madrid, Spain.
Julio ArtiedaUniversity of Navarra, Neuroscience Program CIMA, IdiSNA, Navarra institute for health research, Neurophysiology Service, Clinica Universidad de Navarra, University of Navarra, Pamplona, Spain.
Maria Jesus NicolasNeuroscience Program CIMA, IdiSNA, Navarra institute for health research, University of Navarra, Pamplona, Spain.
Guillermo BesneNeuroscience Program CIMA, IdiSNA, Navarra institute for health research, University of Navarra, Pamplona, Spain.
Maria BunualesGene Therapy Program CIMA, IdiSNA, Navarra institute for health research, University of Navarra, Pamplona, Spain.
Manuela Gonzalez-AparicioGene Therapy Program CIMA, IdiSNA, Navarra institute for health research, University of Navarra, Pamplona, Spain.
Noemi Sola-SevillaDravet Syndrome Unit, Pediatric Neurology Unit, IdiSNA, Navarra institute for health research, University Clinic of Navarra, Pamplona, Spain.
Miguel ValenciaNeuroscience Program CIMA, IdiSNA, Navarra institute for health research, University of Navarra, Pamplona, Spain.ORCID http://orcid.org/0000-0001-5617-5270
Ruben Hernandez-AlcocebaGene Therapy Program CIMA, IdiSNA, Navarra institute for health research, University of Navarra, Pamplona, Spain.
Universidad de Navarra · ESClinica Universidad de Navarra · ESNavarre Institute of Health Research · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID33850219
PMCPMC8044099
OpenAlexW3155213131

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.