A novel compound heterozygous mutation in the GJB2 gene causing non-syndromic hearing loss in a family
Prevalence and audiological profiles of GJB2 mutations in a large collective of hearing impaired patients - ScienceDirect
Spectrum and Frequency of the GJB2 Gene Pathogenic Variants in a Large Cohort of Patients with Hearing Impairment Living in a Subarctic Region of Russia (the Sakha Republic) | PLOS ONE
GJB2 - Wikipedia
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Frontiers | DFNB1 Non-syndromic Hearing Impairment: Diversity of Mutations and Associated Phenotypes
GJB2 - an overview | ScienceDirect Topics
The GJB2 gene mutation profiles in hearing ımpaired patients from Western Turkey, Canakkale
Exome sequencing analysis reveals homozygous GJB2 gene mutation in a Mexican family with profound hearing loss | Revista Médica del Hospital General de México
GJB2 gene therapy and conditional deletion reveal developmental stage-dependent effects on inner ear structure and function: Molecular Therapy - Methods & Clinical Development
SciELO - Brasil - A novel G21R mutation of the GJB2 gene causes autosomal dominant non-syndromic congenital deafness in a Cuban family A novel G21R mutation of the GJB2 gene causes autosomal
Machine learning-based genetic diagnosis models for hereditary hearing loss by the GJB2, SLC26A4 and MT-RNR1 variants - eBioMedicine
Genes | Free Full-Text | GJB2 and GJB6 Genetic Variant Curation in an Argentinean Non-Syndromic Hearing-Impaired Cohort
Genes | Free Full-Text | High Rates of Three Common GJB2 Mutations c.516G>C, c.-23+1G>A, c.235delC in Deaf Patients from Southern Siberia Are Due to the Founder Effect
No evidence for clinical utility in investigating the connexin genes GJB2, GJB6 and GJA1 in non-syndromic hearing loss in black Africans
Genetics of hearing loss - YouTube
GJB2‐related hearing loss in central Iran: Review of the spectrum and frequency of gene mutations - Koohiyan - 2020 - Annals of Human Genetics - Wiley Online Library
GJB2 molecular structure and localization. GJB2 gene is localized in... | Download Scientific Diagram
Sequence analysis of the GJB2 gene. (a) Mutations R75Q (c.224G>A;... | Download Scientific Diagram
GJB6 - an overview | ScienceDirect Topics
GJB2 Gene - GeneCards | CXB2 Protein | CXB2 Antibody
Biomolecules | Free Full-Text | Functional Evaluation of a Rare Variant c.516G>C (p.Trp172Cys) in the GJB2 (Connexin 26) Gene Associated with Nonsyndromic Hearing Loss
The GJB2 gene mutation profiles in hearing ımpaired patients from Western Turkey, Canakkale
