Research progress in delineating the pathological mechanisms of GJB2-related hearing loss

Hearing loss is the most common congenital sensory impairment. Mutations or deficiencies of the GJB2 gene are the most common genetic cause of congenital non-syndromic deafness. Pathological changes such as decreased potential in the cochlea, active cochlear amplification disorders, cochlear develop...

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Detalles Bibliográficos
Autores principales: Wang, Yujun, Jin, Yuan, Zhang, Qiong, Xiong, Ying, Gu, Xiang, Zeng, Shan, Chen, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10272732/
https://www.ncbi.nlm.nih.gov/pubmed/37333892
http://dx.doi.org/10.3389/fncel.2023.1208406

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10272732/
https://www.ncbi.nlm.nih.gov/pubmed/37333892
http://dx.doi.org/10.3389/fncel.2023.1208406

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