Virally-expressed connexin26 restores gap junction function in the cochlea of conditional Gjb2 knockout mice

Mutations in GJB2, which codes for the gap junction protein connexin26, are the most common causes of human nonsyndromic hereditary deafness. We inoculated modified adeno-associated viral vectors into the scala media of early postnatal conditional Gjb2 knockout mice to drive exogenous connexin26 exp...

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Detalles Bibliográficos
Autores principales: Yu, Qing, Wang, Yunfeng, Chang, Qing, Wang, Jianjun, Gong, Shushen, Li, Huawei, Lin, Xi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3881370/
https://www.ncbi.nlm.nih.gov/pubmed/24225640
http://dx.doi.org/10.1038/gt.2013.59

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3881370/
https://www.ncbi.nlm.nih.gov/pubmed/24225640
http://dx.doi.org/10.1038/gt.2013.59

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