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...

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Detalles Bibliográficos
Autores principales: Clabout, Thomas, Maes, Laurence, Acke, Frederic, Wuyts, Wim, Van Schil, Kristof, Coucke, Paul, Janssens, Sandra, De Leenheer, Els
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
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

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9859074/
https://www.ncbi.nlm.nih.gov/pubmed/36672845
http://dx.doi.org/10.3390/genes14010105

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