Restoration of connexin26 protein level in the cochlea completely rescues hearing in a mouse model of human connexin30-linked deafness
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference22 articles.
1. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
2. Connexin-26 mutations in sporadic and inherited sensorineural deafness
3. The Role of Connexins in Human Disease
4. A non–syndromic form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q
5. Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus
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