Analysis of GJB6 (Сx30) and GJB3 (Сx31) genes in deaf patients with monoallelic mutations in GJB2 (Сx26) gene in the Sakha Republic (Yakutia)

Research output: Contribution to journal › Article › peer-review

autosomal recessive deafness 1A (DFNB1A), congenital hearing loss, GJB3 (Cx31) gene, GJB6 (Cx30) gene, monoallelic GJB2-mutations, Sakha Republic (Yakutia), с.del(GJB6-D13S1830), ALLELE, VARIANTS, CONNEXIN 26 GENE, HEARING IMPAIRMENT, EPITHELIUM, DEL(GJB6-D13S1830), SERVER, c.del(GJB6-D13S1830), EXPRESSION, LARGE DELETION, RAT COCHLEA

ID: 10093282