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Ultrastructural pathological changes in the cochlear cells of connexin 26 conditional knockout mice
Mutations in the gene of connexin 26 (Cx26) are the most common cause of human non-syndromic hereditary deafness. The pathogenesis of deafness caused by Cx26 remains uncertain. To explore the basic mechanism underlying Cx26 null mutations, ultrastructural changes and a number of marker proteins in t...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
D.A. Spandidos
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3981006/ https://ncbi.nlm.nih.gov/pubmed/23917463 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/mmr.2013.1614 |
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