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
In Vitro Models of GJB2-Related Hearing Loss Recapitulate Ca2+ Transients via a Gap Junction Characteristic of Developing Cochlea - ScienceDirect
Analysis of the GJB2 Gene and its Mutated Protein in Non-Syndromic Hearing Loss Patients of Gilgit-Baltistan
Genes | Free Full-Text | The GJB2 (Cx26) Gene Variants in Patients with Hearing Impairment in the Baikal Lake Region (Russia)
Detected pathogenic and benign variants in the GJB2 gene in patients... | Download Scientific Diagram
About Genetics and Hearing Loss | A Parent's Guide to Genetics and Hearing Loss
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‐related hearing loss in central Iran: Review of the spectrum and frequency of gene mutations - Koohiyan - 2020 - Annals of Human Genetics - Wiley Online Library
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
GJB2-GT - Sensorion
Connexin 26 (GJB2) mutation in an Argentinean patient with keratitis-ichthyosis-deafness (KID) syndrome: a case report | BMC Medical Genetics | Full Text
a) Location of the GJB2 and GJB6 genes on chromosome 13. (b) The eight... | 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
The GJB2 gene mutation profiles in hearing ımpaired patients from Western Turkey, Canakkale
The GJB2 gene mutation profiles in hearing ımpaired patients from Western Turkey, Canakkale
GJB2 Gene - GeneCards | CXB2 Protein | CXB2 Antibody
Frontiers | DFNB1 Non-syndromic Hearing Impairment: Diversity of Mutations and Associated Phenotypes
A novel compound heterozygous mutation in the GJB2 gene causing non-syndromic hearing loss in a family
GJB2 Gene - GeneCards | CXB2 Protein | CXB2 Antibody
GJB2 - an overview | ScienceDirect Topics
GJB2 - an overview | ScienceDirect Topics
