Molecular study in Brazilian cochlear im
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Thalita Vitachi Christiani; Fabiana Alexandrino; Camila AndrΓ©a de Oliveira; Regi
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Article
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2007
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John Wiley and Sons
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English
β 74 KB
## Abstract The most common form of nonβsyndromic autosomal recessive deafness (NSRD) is caused by mutations in the __GJB2__ gene. Recently, a deletion truncating the __GJB6__ gene, called del(__GJB6β__D13S1830) has also been described normally accompanying mutations in another allele of the __GJB2