Mutations inGJB2,GJB6, and mitochondrial DNA are rare in African American and Caribbean Hispanic individuals with hearing impairment
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference37 articles.
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3. Nonsyndromal profound genetic deafness in childhood;Cremers;Ann NY Acad Sci,1991
4. A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 nonsyndromic hearing impairment;del Castillo;J Med Genet,2005
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