Connexin30-Deficiency Causes Mild Hearing Loss With the Reduction of Endocochlear Potential and ATP Release

GJB2 and GJB6 are adjacent genes encoding connexin 26 (Cx26) and connexin 30 (Cx30), respectively, with overlapping expressions in the inner ear. Both genes are associated with the commonest monogenic hearing disorder, recessive isolated deafness DFNB1. Cx26 plays an important role in auditory devel...

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Detalles Bibliográficos
Autores principales: Chen, Junmin, Chen, Penghui, He, Baihui, Gong, Tianyu, Li, Yue, Zhang, Jifang, Lv, Jingrong, Mammano, Fabio, Hou, Shule, Yang, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Cellular Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8802669/
https://www.ncbi.nlm.nih.gov/pubmed/35110999
http://dx.doi.org/10.3389/fncel.2021.819194

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8802669/
https://www.ncbi.nlm.nih.gov/pubmed/35110999
http://dx.doi.org/10.3389/fncel.2021.819194

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