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

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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Bibliographic Details
Main Authors: Kevin Y. Zhan, Oliver F. Adunka, Adrien Eshraghi, William J. Riggs, Sandra M. Prentiss, Denise Yan, Fred F. Telischi, Xuezhong Liu, Shuman He
Format: Article
Language:English
Published: Elsevier 2021-01-01
Series:Journal of Otology
Subjects:
Electrophysiology
Genetics
Hearing loss
ECAP
ECocHG
Online Access:http://www.sciencedirect.com/science/article/pii/S1672293020300635

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http://www.sciencedirect.com/science/article/pii/S1672293020300635

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