Updated carrier rates for c.35delG (GJB2) associated with hearing loss in Russia and common c.35delG haplotypes in Siberia

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

Deafness, GJB2, c.35delG, Haplotypes, Siberia, European Continental Ancestry Group/genetics, Hearing Loss/genetics, Mutation/genetics, Europe, Humans, Genotype, Haplotypes/genetics, Deafness/genetics, Gene Frequency/genetics, Russia, Middle East, Homozygote, Polymorphism, Single Nucleotide/genetics, Connexins/genetics, Alleles, Heterozygote, 35DELG MUTATION, CX26 GENE, RECESSIVE DEAFNESS, ASHKENAZI JEWS, FOUNDER, CONGENITAL DEAFNESS, CONNEXIN-26 35DELG, HIGH PREVALENCE, GENE MUTATION, GJB2, ANCESTRAL HAPLOTYPE, c.35delG

ID: 17116701