Compound heterozygosity for dominant and recessiveGJB2 mutations: Effect on phenotype and review of the literature
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference34 articles.
1. Functional Analysis of a Dominant Mutation of Human Connexin26 Associated with Nonsyndromic Deafness
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3. Targeted Ablation of Connexin26 in the Inner Ear Epithelial Gap Junction Network Causes Hearing Impairment and Cell Death
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