Detected pathogenic and benign variants in the GJB2 gene in patients... | Download Scientific Diagram
Biology | Free Full-Text | Molecular Mechanisms and Clinical Phenotypes of GJB2 Missense Variants
Genes | Free Full-Text | The GJB2 (Cx26) Gene Variants in Patients with Hearing Impairment in the Baikal Lake Region (Russia)
A novel compound heterozygous mutation in the GJB2 gene causing non-syndromic hearing loss in a family
GJB2 - an overview | ScienceDirect Topics
GJB2 - an overview | ScienceDirect Topics
GJB2 gene therapy and conditional deletion reveal developmental stage-dependent effects on inner ear structure and function: Molecular Therapy - Methods & Clinical Development
GJB2 - an overview | ScienceDirect Topics
GJB2 - Wikipedia
The GJB2 gene mutation profiles in hearing ımpaired patients from Western Turkey, Canakkale
In Vitro Models of GJB2-Related Hearing Loss Recapitulate Ca2+ Transients via a Gap Junction Characteristic of Developing Cochlea - ScienceDirect
Deafness Gene GJB2 Edited in Human Eggs | The Scientist Magazine®
Exome sequencing analysis reveals homozygous GJB2 gene mutation in a Mexican family with profound hearing loss | Revista Médica del Hospital General de México
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
The GJB2 gene mutation profiles in hearing ımpaired patients from Western Turkey, Canakkale
GBW09122 Plasmid DNA of deafness GJB2 gene reference material - National Sharing Platform for Reference Materials
GJB2-GT - Sensorion
Frontiers | DFNB1 Non-syndromic Hearing Impairment: Diversity of Mutations and Associated Phenotypes
A common founder for the 35delG GJB2gene mutation in connexin 26 hearing impairment | Journal of Medical Genetics
Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations | Journal of Human Genetics
GJB2 molecular structure and localization. GJB2 gene is localized in... | Download Scientific Diagram
Connexin 26 (GJB2) mutation in an Argentinean patient with keratitis-ichthyosis-deafness (KID) syndrome: a case report | BMC Medical Genetics | Full Text
Analysis of the GJB2 Gene and its Mutated Protein in Non-Syndromic Hearing Loss Patients of Gilgit-Baltistan
