Variability in noise susceptibility in a Swedish population: the role of 35delG mutation in the connexin 26 (GJB2) gene
Author:
Publisher
Informa UK Limited
Subject
Speech and Hearing
Link
http://www.tandfonline.com/doi/pdf/10.1080/16513860410035854
Reference26 articles.
1. Connexin 26 as a Cause of Hereditary Hearing Loss
2. Genetic Epidemiology of Hearing Impairment
3. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
4. Ion Channel Defects in Hereditary Hearing Loss
5. Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene
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