GJB2(Connexin 26) gene mutations among hearing-impaired persons in a Swedish cohort
Author:
Publisher
Informa UK Limited
Subject
Otorhinolaryngology,General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.3109/00016489.2012.701018
Reference20 articles.
1. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
2. Ion Channel Defects in Hereditary Hearing Loss
3. The35delGMutation in the Connexin 26 Gene (GJB2) Associated with Congenital Deafness: European Carrier Frequencies and Evidence for Its Origin in Ancient Greece
4. GJB2 and GJB6 Mutations in 165 Danish Patients Showing Non-Syndromic Hearing Impairment
5. Causes of hearing impairment in the Norwegian paediatric cochlear implant program
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