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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...
| Autores principales: | , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Chinese PLA General Hospital
2021
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| Materias: | |
| 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 |