Evidence map›Paper›PMID 29435658›Full record

ArticleHuman genetics2018

Correction to: The CAPOS mutation in ATP1A3 alters Na/K-ATPase function and results in auditory neuropathy which has implications for management.

Lisbeth Tranebjærg, Nicola Strenzke, Sture Lindholm, Nanna D Rendtorff, Hanne Poulsen, Himanshu Khandelia, Wojciech Kopec, Troels J Brünnich Lyngbye, Christian Hamel, Cecile Delettre and 21 more

Abstract readPublished Erratum
PubMed Publisher
In one paragraph

Article in Human genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Auditory Neuropathy as the Initial Phenotype for Patients WithFrontiers in cell and developmental biology · 2021
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

31 authors.

Lisbeth TranebjærgDepartment of Otorhinolaryngology, Head and Neck Surgery and Audiology, Rigshospitalet/Bispebjerg, Copenhagen, Denmark. tranebjaerg@sund.ku.dk.
Nicola StrenzkeAuditory Systems Physiology Group, InnerEarLab, Department of Otolaryngology, University Medical Center, Göttingen, Germany.
Sture LindholmENT-Department, County Hospital Kalmar, Kalmar, Sweden.
Nanna D RendtorffDepartment of Clinical Genetics, The Kennedy Center, Copenhagen University Hospital, Copenhagen, Denmark.
Hanne PoulsenInstitute of Biomedicine, University of Aarhus, Aarhus, Denmark.
Himanshu KhandeliaMEMPHYS-Center for Biomembrane Physics, University of Southern Denmark, Odense, Denmark.
Wojciech KopecMEMPHYS-Center for Biomembrane Physics, University of Southern Denmark, Odense, Denmark.
Troels J Brünnich LyngbyePediatric Department, Aarhus University Hospital, Aarhus, Denmark.
Christian HamelMaladies Sensorielles Genetiques, CHRU, Montpellier, France.
Cecile DelettreINSERM U1051, Institute for Neurosciences of Montpellier, Montpellier, France.
Beatrice BocquetMaladies Sensorielles Genetiques, CHRU, Montpellier, France.
Michael BilleDepartment of Otorhinolaryngology, Head and Neck Surgery and Audiology, Rigshospitalet/Gentofte Hospital, Hellerup, Denmark.
Hanne H OwenDepartment of Audiology, Aarhus University Hospital, Aarhus, Denmark.
Toke BekDepartment of Ophthalmology, Aarhus University Hospital, Aarhus, Denmark.
Hanne JensenEye Department Glostrup Hospital, Rigshospitalet, The Kennedy Centre, Glostrup, Denmark.
Karen ØstergaardDepartment of Neurology, Aarhus University Hospital and University of Aarhus, Aarhus, Denmark.
Claes MöllerAudiological Research Centre, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.
Linda LuxonDepartment of Neurotology, National Hospital for Neurology, Queen Square, London, WC1N 3BG, UK.
Lucinda CarrDepartment of Neurology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, WC1N 3JH, UK.
Louise WilsonNorth East Thames Regional Genetics Service, Great Ormond Street Hospital for Children NHS Foundation Trust, London, WC1N 3JH, UK.
Kaukab RajputCochlear Implant Department, Great Ormond Street Hospital for Children NHS Foundation Trust, London, WC1N 3JH, UK.
Tony SirimannaDepartment of Audiovestibular Medicine, Great Ormond Street Hospital for Children NHS Foundation Trust, London, WC1N 3JH, UK.
Katherine Harrop-GriffithsNuffield Hearing and Speech Centre, Royal National Throat Nose and Ear Hospital, London, WC1X 8DA, UK.
Shamima RahmanGenetic and Genomic Medicine Programme, UCL Great Ormond Street Institute of Child Health, London, WC1N 1EH, UK.
Barbara VonaInstitute of Human Genetics, Julius Maximilians University Würzburg, Würzburg, Germany.
Julia DollInstitute of Human Genetics, Julius Maximilians University Würzburg, Würzburg, Germany.
Thomas HaafInstitute of Human Genetics, Julius Maximilians University Würzburg, Würzburg, Germany.
Oliver BartschUniversity Medical Centre, Institute of Human Genetics, Johannes Gutenberg University Mainz, Langenbeckstrasse 1, Mainz, Germany.
Hendrik RosewichDivision of Pediatric Neurology, Department of Pediatric and Adolescent Medicine, University Medical Center, Göttingen, Germany.
Tobias MoserInstitute for Auditory Neuroscience and InnerEarLab, University Medical Center, Göttingen, Germany.
Maria Bitner-GlindziczNorth East Thames Regional Genetics Service, Great Ormond Street Hospital for Children NHS Foundation Trust, London, WC1N 3JH, UK. maria.bitner@ucl.ac.uk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The following information was inadvertently omitted in the original publication.

Identifiers

PMID29435658

What OpenQuestion holds

Textmetadata
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.