Synaptojanin2 Mutation Causes Progressive High-frequency Hearing Loss in Mice-Reference-Cited by-同舟云学术

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Synaptojanin2 Mutation Causes Progressive High-frequency Hearing Loss in Mice

Published:2020-09-25 Issue: Volume:14 Page:
ISSN:1662-5102
Container-title:Frontiers in Cellular Neuroscience
language:
Short-container-title:Front. Cell. Neurosci.

Author:

Martelletti Elisa,Ingham Neil J.,Houston Oliver,Pass Johanna C.,Chen Jing,Marcotti Walter,Steel Karen P.

Funder

Biotechnology and Biological Sciences Research Council

Wellcome Trust

Action on Hearing Loss

Publisher

Frontiers Media SA

Subject

Cellular and Molecular Neuroscience

Reference67 articles.

1. The nature of the negative endocochlear potentials produced by anoxia and ethacrynic acid in the rat and guinea-pig;Bosher;J. Physiol.,1979

2. Ultrastructural defects in stereocilia and tectorial membrane in aging mouse and human cochleae;Bullen;J. Neurosci. Res.,2019

3. Spinster homolog 2 (spns2) deficiency causes early onset progressive hearing loss;Chen;PLoS Genet.

4. A reduction in Ptprq associated with specific features of the deafness phenotype of the miR-96 mutant mouse diminuendo;Chen;Eur. J. Neurosci.

5. Functional development of hair cells in the mammalian inner ear;Corns,2014

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3. Rare-variant association analysis reveals known and new age-related hearing loss genes;European Journal of Human Genetics;2023-02-15

4. The Effect of a Pex3 Mutation on Hearing and Lipid Content of the Inner Ear;Cells;2022-10-13

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