QuickView for GJB2;jsessionid=36C8B7F15E94E89657073B9A4DEF6DD7;jsessionid=9AA8F93C7A3C2FAF9852F7FB62A3D478 (gene)

1. Functional Consequences of Pathogenic Variants of the GJB2 Gene (Cx26) Localized in Different Cx26 D…
2. The pathogenesis of common Gjb2 mutations associated with human hereditary deafness in mice.
3. Functional Evaluation of a Rare Variant c.516G>C (p.Trp172Cys) in the GJB2 (Connexin 26) Gene Associ…
4. Hearing Impairment with Monoallelic GJB2 Variants: A GJB2 Cause or Non-GJB2 Cause?
5. 3D Chromatin Organization Involving MEIS1 Factor in the cis-Regulatory Landscape of GJB2.

There were no clinical trials for GJB2;jsessionid=36C8B7F15E94E89657073B9A4DEF6DD7;jsessionid=9AA8F93C7A3C2FAF9852F7FB62A3D478