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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...
Autores principales: | Santarelli, Rosamaria, Scimemi, Pietro, Costantini, Marco, Domínguez-Ruiz, María, Rodríguez-Ballesteros, Montserrat, del Castillo, Ignacio |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2021
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Materias: | |
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 |
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