Degeneration of saccular hair cells caused by MITF gene mutation

BACKGROUND: Waardenburg syndrome (WS) is the consequence of an inherited autosomal dominant mutation which causes the early degeneration of intermediate cells of cochlear stria vascularis (SV) and profound hearing loss. Patients with WS may also experience primary vestibular symptoms. Most of the cu...

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Detalles Bibliográficos
Autores principales: Du, Yi, Ren, Li-li, Jiang, Qing-qing, Liu, Xing-jian, Ji, Fei, Zhang, Yue, Yuan, Shuo-long, Wu, Zi-Ming, Guo, Wei-Wei, Yang, Shi-Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330439/
https://www.ncbi.nlm.nih.gov/pubmed/30635004
http://dx.doi.org/10.1186/s13064-019-0126-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330439/
https://www.ncbi.nlm.nih.gov/pubmed/30635004
http://dx.doi.org/10.1186/s13064-019-0126-0

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