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Mutations of TMC1 cause deafness by disrupting mechanoelectrical transduction
OBJECTIVE: Mutations of transmembrane channel-like 1 gene (TMC1) can cause dominant (DFNA36) or recessive (DFNB7/B11) deafness. In this article, we describe the characteristics of DFNA36 and DFNB7/B11 deafness, the features of the Tmc1 mutant mouse strains, and recent advances in our understanding o...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4176506/ https://ncbi.nlm.nih.gov/pubmed/24933710 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.anl.2014.04.001 |
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