QuickView for GJB2;jsessionid=36C8B7F15E94E89657073B9A4DEF6DD7;jsessionid=5A3BEC42573681A55FD18957874F6951 (gene)

1. The pathogenesis of common Gjb2 mutations associated with human hereditary deafness in mice.
2. Functional Evaluation of a Rare Variant c.516G>C (p.Trp172Cys) in the GJB2 (Connexin 26) Gene Associ…
3. Hearing Impairment with Monoallelic GJB2 Variants: A GJB2 Cause or Non-GJB2 Cause?
4. 3D Chromatin Organization Involving MEIS1 Factor in the cis-Regulatory Landscape of GJB2.
5. A possible role for second-hit postzygotic GJB2 mutation in porokeratotic eccrine ostial and dermal …

There were no clinical trials for GJB2;jsessionid=36C8B7F15E94E89657073B9A4DEF6DD7;jsessionid=5A3BEC42573681A55FD18957874F6951