Connexin 26 variants and auditory neurop
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Xing Cheng; Li Li; Shanda Brashears; Thierry Morlet; San San Ng; Charles Berlin;
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Article
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2005
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John Wiley and Sons
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English
β 136 KB
## Abstract Genetic and auditory studies of 731 children with severeβtoβprofound hearing loss in US schools for the deaf and 46 additional children receiving clinical services for hearing loss ranging from moderate to profound demonstrated that mutations in the connexin 26 (__GJB2__) and connexin 3