Negative Molecular Diagnostics in Non-Syndromic Hearing Loss: What Next?

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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Bibliographic Details
Main Authors: Thomas Clabout, Laurence Maes, Frederic Acke, Wim Wuyts, Kristof Van Schil, Paul Coucke, Sandra Janssens, Els De Leenheer
Format: Article
Language:English
Published: MDPI AG 2022-12-01
Series:Genes
Subjects:
congenital hearing loss
deafness
molecular diagnostics
exome sequencing
<i>STRC</i> gene
Online Access:https://www.mdpi.com/2073-4425/14/1/105

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