Abnormal outer hair cell efferent innervation in Hoxb1-dependent sensorineural hearing loss

Autosomal recessive mutation of HOXB1 and Hoxb1 causes sensorineural hearing loss in patients and mice, respectively, characterized by the presence of higher auditory thresholds; however, the origin of the defects along the auditory pathway is still unknown. In this study, we assessed whether the ab...

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Detalles Bibliográficos
Autores principales: Di Bonito, Maria, Bourien, Jérôme, Tizzano, Monica, Harrus, Anne-Gabrielle, Puel, Jean-Luc, Avallone, Bice, Nouvian, Regis, Studer, Michèle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10516434/
https://www.ncbi.nlm.nih.gov/pubmed/37738262
http://dx.doi.org/10.1371/journal.pgen.1010933

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10516434/
https://www.ncbi.nlm.nih.gov/pubmed/37738262
http://dx.doi.org/10.1371/journal.pgen.1010933

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