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LINKING DEAFNESS GENES TO HAIR-BUNDLE DEVELOPMENT AND FUNCTION
The identification of genes underlying monogenic, early-onset forms of deafness in humans has provided unprecedented insight into the molecular mechanisms of hearing in the peripheral auditory system. The molecules involved in the development and function of the cochlea eluded characterization until...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
2009
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3332156/ https://www.ncbi.nlm.nih.gov/pubmed/19471269 http://dx.doi.org/10.1038/nn.2330 |