Prevalence of the GJB2 mutations and the del(GJB6-D13S1830) mutation in Brazilian patients with deafness
Author:
Publisher
Elsevier BV
Subject
Sensory Systems
Reference46 articles.
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3. Clinical studies of families with hearing loss attributable to mutations in the connexin 26 gene (GJB2/DFNB1);Cohn;Pediatrics,1999
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