Recent insights into gap junction biogenesis in the cochlea
Author:
Affiliation:
1. GIGA‐Neurosciences, Unit of Cell and Tissue Biology University of Liège Liège Belgium
Funder
Fonds De La Recherche Scientifique - FNRS
Publisher
Wiley
Subject
Developmental Biology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/dvdy.538
Reference68 articles.
1. Congenital hearing loss
2. A Deletion Involving the Connexin 30 Gene in Nonsyndromic Hearing Impairment
3. Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus
4. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
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