Mohammad Farhadi
Department and Research Center of ENT & Head and Neck Surgery of Tehran University of Medical Sciences, Tehran, Iran
[ 1 ] - Profile of Iranian GJB2 Mutations in Young Population with Novel Mutation
Objective(s) Despite the enormous heterogeneity of genetic hearing loss, most non-syndromic hearing losses are caused by mutations in the GJB2 gene. We aimed to characterize the mutation profiles of 100 Iranian deaf patients that were under 10 years old. Materials and Methods Patients were tested with direct sequencing of entire coding region of the GJB2 gene. Results Eight known mutations...
نویسندگان همکار