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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Hlavní autoři: Nakanishi, Hiroshi, Kurima, Kiyoto, Kawashima, Yoshiyuki, Griffith, Andrew J.
Médium: Artigo
Jazyk:Inglês
Vydáno: 2014
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On-line přístup: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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