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Connexin30 null and conditional connexin26 null mice display distinct pattern and time course of cellular degeneration in the cochlea
Mutations in connexin26 (Cx26) and Cx30 are the most common cause of non-syndromic inherited deafness in humans. To understand underlying molecular mechanisms, we investigated the pattern and time course of cellular degeneration in the cochlea of conditional Cx26 (cCx26) null and Cx30 null mice. In...
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| Autors principals: | , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2009
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2846422/ https://ncbi.nlm.nih.gov/pubmed/19673007 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/cne.22117 |
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