Indian J Otolaryngol Head Neck Surg
January 2010
Objectives: To identify the prevalence of GJB2 (Cx 26)and GJB6 (Cx 30) mutations in hearing impaired individuals from Western and South India.
Study Design: Cross-sectional study.
Methods: Families with hearing impaired individuals (prelingual, non-syndromic, sensori-neural hearing loss) were enrolled and genomic DNA was extracted.