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New Tmc1 Deafness Mutations Impact Mechanotransduction in Auditory Hair Cells
Transmembrane channel-like protein isoform 1 (TMC1) is a major component of the mechano-electrical transducer (MET) channel in cochlear hair cells and is subject to numerous mutations causing deafness. We report a new dominant human deafness mutation, TMC1 p.T422K, and have characterized the homolog...
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| 出版年: | J Neurosci |
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| 主要な著者: | , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Society for Neuroscience
2021
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| 主題: | |
| オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8152607/ https://ncbi.nlm.nih.gov/pubmed/33824189 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.2537-20.2021 |
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