Connexin26 Mutations Associated With Nonsyndromic Hearing Loss
Author:
Publisher
Wiley
Subject
Otorhinolaryngology
Reference13 articles.
1. Genetic Epidemiology of Hearing Impairment
2. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
3. Connexin-26 mutations in sporadic and inherited sensorineural deafness
4. Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene
5. Connexin-26 mutations in sporadic non-syndromal sensorineural deafness
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