Cochlear Synaptopathy due to Mutations in OTOF Gene May Result in Stable Mild Hearing Loss and Severe Impairment of Speech Perception

Congenital profound hearing loss with preserved cochlear outer hair cell activity (otoacoustic emissions and cochlear microphonic) is the most common phenotype associated with mutations in the OTOF gene. The aim of this study was to investigate the pathophysiological mechanisms behind the auditory d...

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Detalles Bibliográficos
Autores principales: Santarelli, Rosamaria, Scimemi, Pietro, Costantini, Marco, Domínguez-Ruiz, María, Rodríguez-Ballesteros, Montserrat, del Castillo, Ignacio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9973442/
https://www.ncbi.nlm.nih.gov/pubmed/33908410
http://dx.doi.org/10.1097/AUD.0000000000001052

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9973442/
https://www.ncbi.nlm.nih.gov/pubmed/33908410
http://dx.doi.org/10.1097/AUD.0000000000001052

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