Pathological mechanisms of connexin26-related hearing loss: Potassium recycling, ATP-calcium signaling, or energy supply?

Hereditary deafness is one of the most common human birth defects. GJB2 gene mutation is the most genetic etiology. Gap junction protein 26 (connexin26, Cx26) encoded by the GJB2 gene, which is responsible for intercellular substance transfer and signal communication, plays a critical role in hearin...

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Detalles Bibliográficos
Autores principales: Chen, Penghui, Wu, Wenjin, Zhang, Jifang, Chen, Junmin, Li, Yue, Sun, Lianhua, Hou, Shule, Yang, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9520402/
https://www.ncbi.nlm.nih.gov/pubmed/36187349
http://dx.doi.org/10.3389/fnmol.2022.976388

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9520402/
https://www.ncbi.nlm.nih.gov/pubmed/36187349
http://dx.doi.org/10.3389/fnmol.2022.976388

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