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
GJB2 Gene - GeneCards | CXB2 Protein | CXB2 Antibody
GBW09122 Plasmid DNA of deafness GJB2 gene reference material - National Sharing Platform for Reference Materials
Genes | Free Full-Text | GJB2 and GJB6 Genetic Variant Curation in an Argentinean Non-Syndromic Hearing-Impaired Cohort
Connexin 26 (GJB2) mutation in an Argentinean patient with keratitis-ichthyosis-deafness (KID) syndrome: a case report | BMC Medical Genetics | Full Text
![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
GJB2 molecular structure and localization. GJB2 gene is localized in... | Download Scientific Diagram
a) Location of the GJB2 and GJB6 genes on chromosome 13. (b) The eight... | Download Scientific Diagram
No evidence for clinical utility in investigating the connexin genes GJB2, GJB6 and GJA1 in non-syndromic hearing loss in black Africans
A novel compound heterozygous mutation in the GJB2 gene causing non-syndromic hearing loss in a family
About Genetics and Hearing Loss | A Parent's Guide to Genetics and Hearing Loss
Frontiers | GJB2 Mutations Linked to Hearing Loss Exhibit Differential Trafficking and Functional Defects as Revealed in Cochlear-Relevant Cells
Exome sequencing analysis reveals homozygous GJB2 gene mutation in a Mexican family with profound hearing loss | Revista Médica del Hospital General de México
GJB2 - an overview | ScienceDirect Topics
A common founder for the 35delG GJB2gene mutation in connexin 26 hearing impairment | Journal of Medical Genetics
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
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
Detected pathogenic and benign variants in the GJB2 gene in patients... | Download Scientific Diagram
Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations | Journal of Human Genetics
Analysis of the GJB2 Gene and its Mutated Protein in Non-Syndromic Hearing Loss Patients of Gilgit-Baltistan
Biology | Free Full-Text | Molecular Mechanisms and Clinical Phenotypes of GJB2 Missense Variants
Connexin 26 Gene Linked To Sensorineural Hearing Loss
