Frequency and distribution of GJB2 (connexin 26) and GJB6 (connexin 30) mutations in a large North American repository of deaf probands
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical)
Reference32 articles.
1. GJB2 (connexin 26) variants and nonsyndromic sensorineural hearing loss: A HuGE review
2. Genetic epidemiological studies of early-onset deafness in the U.S. school-age population
3. Genetic Epidemiology of Hearing Impairment
4. Genetic Causes of Hearing Loss
5. Phenotypic variation in Waardenburg syndrome: mutational heterogeneity, modifier genes or polygenic background?
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