Electrophysiology and genetic testing in the precision medicine of congenital deafness: A review

BACKGROUND: Congenital hearing loss is remarkably heterogeneous, with over 130 deafness genes and thousands of variants, making for innumerable genotype/phenotype combinations. Understanding both the pathophysiology of hearing loss and molecular site of lesion along the auditory pathway permits for...

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Detalles Bibliográficos
Autores principales: Zhan, Kevin Y., Adunka, Oliver F., Eshraghi, Adrien, Riggs, William J., Prentiss, Sandra M., Yan, Denise, Telischi, Fred F., Liu, Xuezhong, He, Shuman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chinese PLA General Hospital 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7814082/
https://www.ncbi.nlm.nih.gov/pubmed/33505449
http://dx.doi.org/10.1016/j.joto.2020.07.003

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7814082/
https://www.ncbi.nlm.nih.gov/pubmed/33505449
http://dx.doi.org/10.1016/j.joto.2020.07.003

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