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
Five-family pedigree. The graphic depicts GJB2 gene mutations (A-E).... | Download Scientific Diagram
In Vitro Models of GJB2-Related Hearing Loss Recapitulate Ca2+ Transients via a Gap Junction Characteristic of Developing Cochlea - ScienceDirect
Detected pathogenic and benign variants in the GJB2 gene in patients... | Download Scientific Diagram
GJB2 - Wikipedia
GJB2 Gene - GeneCards | CXB2 Protein | CXB2 Antibody
Genetics of hearing loss - YouTube
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 - an overview | ScienceDirect Topics
The GJB2 gene mutation profiles in hearing ımpaired patients from Western Turkey, Canakkale
Frontiers | GJB2 Mutations Linked to Hearing Loss Exhibit Differential Trafficking and Functional Defects as Revealed in Cochlear-Relevant Cells
GJB2 - an overview | ScienceDirect Topics
A novel compound heterozygous mutation in the GJB2 gene causing non-syndromic hearing loss in a family
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
No evidence for clinical utility in investigating the connexin genes GJB2, GJB6 and GJA1 in non-syndromic hearing loss in black Africans
Connexin 26 Gene Linked To Sensorineural Hearing Loss
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
Biology | Free Full-Text | Molecular Mechanisms and Clinical Phenotypes of GJB2 Missense Variants
GJB2 gene therapy and conditional deletion reveal developmental stage-dependent effects on inner ear structure and function: Molecular Therapy - Methods & Clinical Development
About Genetics and Hearing Loss | A Parent's Guide to Genetics and Hearing Loss
Genes | Free Full-Text | GJB2 and GJB6 Genetic Variant Curation in an Argentinean Non-Syndromic Hearing-Impaired Cohort
Genes | Free Full-Text | The GJB2 (Cx26) Gene Variants in Patients with Hearing Impairment in the Baikal Lake Region (Russia)
Analysis of the GJB2 Gene and its Mutated Protein in Non-Syndromic Hearing Loss Patients of Gilgit-Baltistan
GJB2-GT - Sensorion
GJB2 - an overview | ScienceDirect Topics
