In Vitro Models of GJB2-Related Hearing Loss Recapitulate Ca2+ Transients via a Gap Junction Characteristic of Developing Cochlea - ScienceDirect
About Genetics and Hearing Loss | A Parent's Guide to Genetics and Hearing Loss
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
Analysis of the GJB2 Gene and its Mutated Protein in Non-Syndromic Hearing Loss Patients of Gilgit-Baltistan
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
Connexin 26 Gene Linked To Sensorineural Hearing Loss
GJB2 - an overview | ScienceDirect Topics
Biology | Free Full-Text | Molecular Mechanisms and Clinical Phenotypes of GJB2 Missense Variants
The GJB2 gene mutation profiles in hearing ımpaired patients from Western Turkey, Canakkale
A common founder for the 35delG GJB2gene mutation in connexin 26 hearing impairment | Journal of Medical Genetics
Analysis of the GJB2 Gene and its Mutated Protein in Non-Syndromic Hearing Loss Patients of Gilgit-Baltistan
The GJB2 gene mutation profiles in hearing ımpaired patients from Western Turkey, Canakkale
Detected pathogenic and benign variants in the GJB2 gene in patients... | Download Scientific Diagram
GJB2 Gene - GeneCards | CXB2 Protein | CXB2 Antibody
GJB2 gene therapy and conditional deletion reveal developmental stage-dependent effects on inner ear structure and function: Molecular Therapy - Methods & Clinical Development
Genes | Free Full-Text | The GJB2 (Cx26) Gene Variants in Patients with Hearing Impairment in the Baikal Lake Region (Russia)
GJB2 - an overview | ScienceDirect Topics
Exome sequencing analysis reveals homozygous GJB2 gene mutation in a Mexican family with profound hearing loss | Revista Médica del Hospital General de México
Five-family pedigree. The graphic depicts GJB2 gene mutations (A-E).... | Download Scientific Diagram
![PDF] The role of gene GJB2 and connexin 26 in hearing impairment | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/b8c363ff64513fc0aff91cab24d4527db327d388/2-Figure1-1.png "PDF] The role of gene GJB2 and connexin 26 in hearing impairment | Semantic Scholar")
PDF] The role of gene GJB2 and connexin 26 in hearing impairment | Semantic Scholar
Frontiers | GJB2 Mutations Linked to Hearing Loss Exhibit Differential Trafficking and Functional Defects as Revealed in Cochlear-Relevant Cells
GJB2 molecular structure and localization. GJB2 gene is localized in... | Download Scientific Diagram
Genes | Free Full-Text | GJB2 and GJB6 Genetic Variant Curation in an Argentinean Non-Syndromic Hearing-Impaired Cohort
Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations | Journal of Human Genetics
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
