Prevalence of GJB2 (CX26) gene mutations in south Iranian patients with autosomal recessive nonsyndromic sensorineural hearing loss

Prevalence of Connexin 26 (GJB2) and Pendred (SLC26A4) Mutations in a Population of Adult Cochlear Implant Candidates

(2010) Jordan B. Hochman et al.   OTOLOGY & NEUROTOLOGY

Two Novel Missense Mutations in the Connexin 26 Gene in Turkish Patients with Nonsyndromic Hearing Loss

(2009) Akin Yilmaz et al.   BIOCHEMICAL GENETICS

Mutation Analysis of Familial GJB2-Related Deafness in Iranian Azeri Turkish Patients

(2009) Mortaza Bonyadi et al.   Genetic Testing and Molecular Biomarkers

Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China

(2009) Yongyi Yuan et al.   Journal of Translational Medicine

Gap junctions and connexins in the inner ear: their roles in homeostasis and deafness

(2008) Regina Nickel et al.   Current Opinion in Otolaryngology & Head and Neck Surgery

GJB2 mutations in Baluchi population

(2008) Anoosh Naghavi et al.   JOURNAL OF GENETICS