Mutation spectrum of the connexin 26 (GJB2) gene in Taiwanese patients with prelingual deafness
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical)
Reference33 articles.
1. Genetic Epidemiology of Hearing Impairment
2. Epidemiology of Permanent Childhood Hearing Impairment in Trent Region, 1985–1993
3. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
4. Gap Junction Systems in the Rat Vestibular Labyrinth: Immunohistochemical and Ultrastructural Analysis
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