Scientists map genetic blueprint for childhood deafness, paving way for future cures
NCT ID NCT04202185
Summary
This study aimed to better understand a specific genetic cause of profound childhood deafness called DFNB9. Researchers followed 150 children with severe hearing loss to collect detailed hearing tests and genetic information. The goal was to create a database to improve diagnosis and identify the best candidates for potential future gene therapy treatments.
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Contacts and locations
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Locations
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Unité d'Audiophonologie et d'Implantation cochléaire - Necker hospital
Paris, 75015, France
Conditions
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