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...
Main Authors: | , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Elsevier
2021-01-01
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Series: | Journal of Otology |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S1672293020300635 |