subject area of
- 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.