Functional Study of GJB2 in Hereditary Hearing Loss
Author:
Publisher
Wiley
Subject
Otorhinolaryngology
Reference21 articles.
1. Newborn Hearing Screening: The Great Omission
2. Genetic Epidemiology of Hearing Impairment
3. Connexin26 mutations associated with the most common form of non- syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans
4. Connexin-26 mutations in sporadic and inherited sensorineural deafness
5. Clinical Studies of Families With Hearing Loss Attributable to Mutations in the Connexin 26 Gene (GJB2/DFNB1)
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