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...

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Detalles Bibliográficos
Autores principales: Petit, Christine, Richardson, Guy P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2009
Materias:
Article
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

Internet

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

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