Evidence map›Paper›PMID 38983270›Full record

ArticleFrontiers in genetics2024

Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health.

Rahma Mkaouar, Zied Riahi, Jihene Marrakchi, Nessrine Mezzi, Lilia Romdhane, Maroua Boujemaa, Hamza Dallali, Marwa Sayeb, Saida Lahbib, Hajer Jaouadi and 23 more

Abstract readPublished Erratum
PubMed Full text at PMC Publisher
In one paragraph

Article in Frontiers in genetics, 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

5 · Who and what money

Authors and funding

33 authors.

Rahma MkaouarLaboratory of Biomedical Genomics and Oncogenetics LR16IPT05, Pasteur Institute in Tunis, University of Tunis El Manar, Tunis, Tunisia.
Zied RiahiLaboratory of Biomedical Genomics and Oncogenetics LR16IPT05, Pasteur Institute in Tunis, University of Tunis El Manar, Tunis, Tunisia.
Jihene MarrakchiLaboratory of Biomedical Genomics and Oncogenetics LR16IPT05, Pasteur Institute in Tunis, University of Tunis El Manar, Tunis, Tunisia.
Nessrine MezziLaboratory of Biomedical Genomics and Oncogenetics LR16IPT05, Pasteur Institute in Tunis, University of Tunis El Manar, Tunis, Tunisia.
Lilia RomdhaneLaboratory of Biomedical Genomics and Oncogenetics LR16IPT05, Pasteur Institute in Tunis, University of Tunis El Manar, Tunis, Tunisia.
Maroua BoujemaaLaboratory of Biomedical Genomics and Oncogenetics LR16IPT05, Pasteur Institute in Tunis, University of Tunis El Manar, Tunis, Tunisia.
Hamza DallaliLaboratory of Biomedical Genomics and Oncogenetics LR16IPT05, Pasteur Institute in Tunis, University of Tunis El Manar, Tunis, Tunisia.
Marwa SayebLaboratory of Biomedical Genomics and Oncogenetics LR16IPT05, Pasteur Institute in Tunis, University of Tunis El Manar, Tunis, Tunisia.
Saida LahbibLaboratory of Biomedical Genomics and Oncogenetics LR16IPT05, Pasteur Institute in Tunis, University of Tunis El Manar, Tunis, Tunisia.
Hajer JaouadiLaboratory of Biomedical Genomics and Oncogenetics LR16IPT05, Pasteur Institute in Tunis, University of Tunis El Manar, Tunis, Tunisia.
Hela BoudabbousDepartment of Pediatrics, La Rabta Hospital, Tunis, Tunisia.
Lotfi ZekriLaboratory of Biomedical Genomics and Oncogenetics LR16IPT05, Pasteur Institute in Tunis, University of Tunis El Manar, Tunis, Tunisia.
Mariem CharguiLaboratory of Biomedical Genomics and Oncogenetics LR16IPT05, Pasteur Institute in Tunis, University of Tunis El Manar, Tunis, Tunisia.
Olfa MessaoudLaboratory of Biomedical Genomics and Oncogenetics LR16IPT05, Pasteur Institute in Tunis, University of Tunis El Manar, Tunis, Tunisia.
Meriem ElyounsiDepartment of Congenital and Hereditary Diseases, Charles Nicolle Hospital in Tunis, Tunis, Tunisia.
Ichraf KraouaChild and Adolescent Neurology Department of Neurology, National Institute of Neurology, Tunis, Tunisia.
Anissa ZaouakDepartment of Dermatology, Habib Thameur Hospital, Research Unit Genodermatoses and Cancers LR12SP03, Tunis, Tunisia.
Ilhem TurkiChild and Adolescent Neurology Department of Neurology, National Institute of Neurology, Tunis, Tunisia.
Mourad MokniService de dermatologie, Hôpital La Rabta, Unité de recherche UR 12SP07, Hôpital La Rabta, Tunis, Tunisia.
Sophie BoucherService d'ORL et chirurgie cervico-faciale, CHU d'Angers, Angers, France.
Christine PetitInstitut Pasteur, Université Paris Cité, Inserm UA06, Institut de l'Audition, Paris, France.
Fabrice GiraudetUnité Mixte de Recherche (UMR) 1107, INSERM, Clermont-Ferrand, France.
Chiraz MbarekENT Department, Habib Thameur Hospital, Tunis, Tunisia.
Ghazi BesbesDepartment of Otorhinolaryngology and Maxillofacial Surgery-La Rabta Hospital in Tunis, Tunis, Tunisia.
Soumeyya HalayemLaboratory of Biomedical Genomics and Oncogenetics LR16IPT05, Pasteur Institute in Tunis, University of Tunis El Manar, Tunis, Tunisia.
Rim ZainineLaboratory of Biomedical Genomics and Oncogenetics LR16IPT05, Pasteur Institute in Tunis, University of Tunis El Manar, Tunis, Tunisia.
Hamida TurkiDermatology Department Hedi Chaker University Hospital, Sfax University Sfax Tunisia, Tunis, Tunisia.
Amel TounsiCNSS Polyclinic, Bizerte, Tunisia.
Crystel BonnetInstitut Pasteur, Université Paris Cité, Inserm UA06, Institut de l'Audition, Paris, France.
Ridha MradDepartment of Congenital and Hereditary Diseases, Charles Nicolle Hospital in Tunis, Tunis, Tunisia.
Sonia AbdelhakLaboratory of Biomedical Genomics and Oncogenetics LR16IPT05, Pasteur Institute in Tunis, University of Tunis El Manar, Tunis, Tunisia.
Mediha TrabelsiDepartment of Congenital and Hereditary Diseases, Charles Nicolle Hospital in Tunis, Tunis, Tunisia.
Cherine CharfeddineLaboratory of Biomedical Genomics and Oncogenetics LR16IPT05, Pasteur Institute in Tunis, University of Tunis El Manar, Tunis, Tunisia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

[This corrects the article DOI: 10.3389/fgene.2024.1384094.].

Indexed as

early detectionnext-generation sequencing (NGS)spectrum of SDssyndromic deafness (SD)Tunisiaunder-diagnosis

Identifiers

PMID38983270
PMCPMC11231432

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.