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