https://experts.arizona.edu/en/publications/a-prospective-longitudinal-study-of-the-impact-of-gjb2gjb6-geneti/
A prospective, longitudinal study of the impact of GJB2/GJB6 genetic testing on the beliefs and...
https://morl.lab.uiowa.edu/clinical-diagnostic-services/hearing-loss-clinical-division/gjb2gjb6-connexin-2630
GJB2/GJB6 (Connexin 26/30) | Molecular Otolaryngology and Renal Research Laboratories - The...
GJB2-related autosomal recessive non-syndromic hearing loss is the most common genetic cause of congenital severe-to-profound non-progressive sensorineural...
https://pubmed.ncbi.nlm.nih.gov/39162005/
GJB2 Promotes HCC Progression by Activating Glycolysis Through Cytoplasmic Translocation and...
Despite substantial breakthroughs in the treatment of hepatocellular carcinoma (HCC) in recent years, many patients are diagnosed in the middle or late stages,...
promoteshccprogression
https://pubmed.ncbi.nlm.nih.gov/25649612/
GJB2 as Well as SLC26A4 Gene Mutations are Prominent Causes for Congenital Deafness
Mutations in gap junction proteins encoding beta connexions are believed to be a major cause for congenital hearing loss. The purpose of this study was to do...