Hearing Loss and Connexin 26
Author:
Affiliation:
1. Department of Otorhinolaryngology, University Medical Centre St Radboud, Nijmegen, The Netherlands
2. Department of Medical Genetics, University Medical Centre St Radboud, Nijmegen, The Netherlands
Publisher
SAGE Publications
Subject
General Medicine
Link
http://journals.sagepub.com/doi/pdf/10.1177/014107680209500403
Reference21 articles.
1. Genetic Epidemiology of Hearing Impairment
2. Genetic deafness.
3. Hearing disorders in childhood, some procedures for detection, identification and diagnostic evaluation
4. Clinical phenotype and mutations in connexin 26 (DFNB1/GJB2), the most common cause of childhood hearing loss
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1. Programming Levels and Speech Perception in Pediatric Cochlear Implant Recipients With Enlarged Vestibular Aqueduct or GJB2 Mutation;Otology & Neurotology;2023-06
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3. Genetic Determinants of Non-Syndromic Enlarged Vestibular Aqueduct: A Review;Audiology Research;2021-08-28
4. Molecular alteration in the Gap Junction Beta 2 (GJB2) gene associated with non-syndromic sensorineural hearing impairment;Intractable & Rare Diseases Research;2021-02-28
5. Auditory Detection Thresholds and Cochlear Resistivity Differ Between Pediatric Cochlear Implant Listeners With Enlarged Vestibular Aqueduct and Those With Connexin-26 Mutations;American Journal of Audiology;2020-03-05
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