Transcription, Translation, and Transitions
Deafness Genes and Their Diagnostic Applications
Mutation in Mitochondrial DNA as a Cause of Presbyacusis
A Novel Mutation Identified in the DFNA5 Gene in a Dutch Family
A Novel Connexin 26 Mutation Associated with Autosomal Recessive Sensorineural Deafness
Sex-Related Hearing Impairment in Wolfram Syndrome Patients Identified by Inactivating WFS1 Mutations
Conference Calendar