Sensorineural Hearing Loss and Mitochondrial Apoptosis of Cochlear Spiral Ganglion Neurons in Fibroblast Growth Factor 13 Knockout Mice

Deafness is known to occur in more than 400 syndromes and accounts for almost 30% of hereditary hearing loss. The molecular mechanisms underlying such syndromic deafness remain unclear. Furthermore, deafness has been a common feature in patients with three main syndromes, the BÖrjeson-Forssman-Lehma...

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Detalles Bibliográficos
Autores principales: Yu, Yulou, Yang, Jing, Luan, Feng, Gu, Guoqiang, Zhao, Ran, Wang, Qiong, Dong, Zishan, Tang, Junming, Wang, Wei, Sun, Jinpeng, Lv, Ping, Zhang, Hailin, Wang, Chuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8242186/
https://www.ncbi.nlm.nih.gov/pubmed/34220452
http://dx.doi.org/10.3389/fncel.2021.658586

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8242186/
https://www.ncbi.nlm.nih.gov/pubmed/34220452
http://dx.doi.org/10.3389/fncel.2021.658586

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