Temporal Bone Imaging in GJB2 Deafness
Author:
Publisher
Wiley
Subject
Otorhinolaryngology
Reference15 articles.
1. Clinical Studies of Families With Hearing Loss Attributable to Mutations in the Connexin 26 Gene (GJB2/DFNB1)
2. Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling
3. Audiological Manifestations and Features of Connexin 26 Deafness
4. A Diagnostic Paradigm for Childhood Idiopathic Sensorineural Hearing Loss
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4. Functional Testing of SLC26A4 Variants—Clinical and Molecular Analysis of a Cohort with Enlarged Vestibular Aqueduct from Austria;International Journal of Molecular Sciences;2018-01-10
5. DFNB1 Non-syndromic Hearing Impairment: Diversity of Mutations and Associated Phenotypes;Frontiers in Molecular Neuroscience;2017-12-22
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