Literature DB >> 24010186

Genetic deafness of central origin.

M S Deol1, M P Frank, K P Steel, G R Bock.   

Abstract

The autosomal recessive gene quivering in the mouse causes deafness. The cochlea in mutant animals is histologically normal, and the thresholds for compound action potentials at the round window are also normal. But the thresholds for potentials in the inferior colliculus are significantly higher in mutant animals than in normal ones, showing that the cause of deafness is retrocochlear. This mutant is believed to be the first proven instance of genetic deafness of central origin.

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Year:  1983        PMID: 24010186     DOI: 10.1016/0006-8993(83)91248-9

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  3 in total

Review 1.  Decreased temporal precision of neuronal signaling as a candidate mechanism of auditory processing disorder.

Authors:  Conny Kopp-Scheinpflug; Bruce L Tempel
Journal:  Hear Res       Date:  2015-06-25       Impact factor: 3.208

2.  A recessive mutation in beta-IV-spectrin (SPTBN4) associates with congenital myopathy, neuropathy, and central deafness.

Authors:  Ellen Knierim; Esther Gill; Franziska Seifert; Susanne Morales-Gonzalez; Sathya D Unudurthi; Thomas J Hund; Werner Stenzel; Markus Schuelke
Journal:  Hum Genet       Date:  2017-05-24       Impact factor: 4.132

3.  Loss of β4-spectrin impairs Nav channel clustering at the heminode and temporal fidelity of presynaptic spikes in developing auditory brain.

Authors:  Kaila Nip; Sean Kashiwagura; Jun Hee Kim
Journal:  Sci Rep       Date:  2022-04-07       Impact factor: 4.379

  3 in total

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