Evidence map›Paper›PMID 31097876›Full record

ArticleCanadian journal of veterinary research = Revue canadienne de recherche veterinaire2019

A missense mutation in MYO7A is associated with bilateral deafness and vestibular dysfunction in the Doberman pinscher breed.

Aubrey A Webb, Alison L Ruhe, Mark W Neff

Abstract read
In one paragraph

Article in Canadian journal of veterinary research = Revue canadienne de recherche veterinaire, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

11 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Identification of a novel compound heterozygous pathogenic variant inThe Journal of international medical research · 2023
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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

3 authors at 1 institution in 1 country.

Aubrey A WebbCullenWebb Animal Eye Specialists, Riverview, New-Brunswick E1B 4X2 (Webb); Department of Clinical Neurosciences, University of Calgary, Calgary, Alberta T2N 1N4 (Webb); ProjectDog, Davis, California 95616, USA (Ruhe); Van Andel Research Institute, Grand Rapids, Michigan 49503, USA (Ruhe, Neff); Translational Genomics Research Institute, Phoenix, Arizona 85004, USA (Neff).
Alison L RuheCullenWebb Animal Eye Specialists, Riverview, New-Brunswick E1B 4X2 (Webb); Department of Clinical Neurosciences, University of Calgary, Calgary, Alberta T2N 1N4 (Webb); ProjectDog, Davis, California 95616, USA (Ruhe); Van Andel Research Institute, Grand Rapids, Michigan 49503, USA (Ruhe, Neff); Translational Genomics Research Institute, Phoenix, Arizona 85004, USA (Neff).
Mark W NeffCullenWebb Animal Eye Specialists, Riverview, New-Brunswick E1B 4X2 (Webb); Department of Clinical Neurosciences, University of Calgary, Calgary, Alberta T2N 1N4 (Webb); ProjectDog, Davis, California 95616, USA (Ruhe); Van Andel Research Institute, Grand Rapids, Michigan 49503, USA (Ruhe, Neff); Translational Genomics Research Institute, Phoenix, Arizona 85004, USA (Neff).
Van Andel Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bilateral deafness with concurrent vestibular dysfunction was first reported in the Doberman pinscher in 1980. Here, we identify a coding mutation in the MYO7A gene that is perfectly associated with the disorder. The lack of visual deficits in affected dogs suggests that, like rodents but unlike humans, MYO7A is not required for retinal function. DNA testing of the mutation will enable dog breeders to manage the incidence of this genetic defect.

Indexed as

Genetic Predisposition to DiseaseMutation, MissenseAnimalsCase-Control StudiesDeafnessDNADog DiseasesDogsGene Expression RegulationGenome-Wide Association StudyGenotypeMyosinsMyosin VIIaVestibular DiseasesWhole Genome SequencingDNAMYO7A protein, humanMyosinsMyosin VIIa

Identifiers

PMID31097876
PMCPMC6450158
OpenAlexW2954821473

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.