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• Connexin-related (DFNB1) hearing loss: is routine computed tomography imaging necessary? 
• Identification of aberrantly regulated genes in diseased skin using the cDNA differential display technique. 
• Loss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model. 
• Prevalence of mutations in GJB2, SLC26A4, and mtDNA in children with severe or profound sensorineural hearing loss in southwestern China.