Degradation of cochlear Connexin26 accelerate the development of age‐related hearing loss

The GJB2 gene, encoding Connexin26 (Cx26), is one of the most common causes of inherited deafness. Clinically, mutations in GJB2 cause congenital deafness or late‐onset progressive hearing loss. Recently, it has been reported that Cx26 haploid deficiency accelerates the development of age‐related he...

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Detalles Bibliográficos
Autores principales: Xu, Kai, Chen, Sen, Bai, Xue, Xie, Le, Qiu, Yue, Liu, Xiao‐zhou, Wang, Xiao‐hui, Kong, Wei‐jia, Sun, Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10652327/
https://www.ncbi.nlm.nih.gov/pubmed/37681746
http://dx.doi.org/10.1111/acel.13973

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10652327/
https://www.ncbi.nlm.nih.gov/pubmed/37681746
http://dx.doi.org/10.1111/acel.13973

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