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Clarin-1 acts as a modulator of mechanotransduction activity and presynaptic ribbon assembly
Clarin-1 is a four-transmembrane protein expressed by hair cells and photoreceptors. Mutations in its corresponding gene are associated with Usher syndrome type 3, characterized by late-onset and progressive hearing and vision loss in humans. Mice carrying mutations in the clarin-1 gene have hair bu...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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The Rockefeller University Press
2014
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4226736/ https://www.ncbi.nlm.nih.gov/pubmed/25365995 http://dx.doi.org/10.1083/jcb.201404016 |