Cargando…
Negative Molecular Diagnostics in Non-Syndromic Hearing Loss: What Next?
Congenital hearing loss has an impact on almost every facet of life. In more than 50% of cases, a genetic cause can be identified. Currently, extensive genetic testing is available, although the etiology of some patients with obvious familial hearing loss remains unknown. We selected a cohort of mut...
| Autores principales: | , , , , , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
MDPI
2022
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9859074/ https://www.ncbi.nlm.nih.gov/pubmed/36672845 http://dx.doi.org/10.3390/genes14010105 |