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Connexin 26
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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 …
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Connexin Genotypes in Cystic Fibrosis
The Prevalence of Hearing Loss Among Children With Congenital Hypothyroidism
Valganciclovir Therapy in Infants and Children With Congenital CMV Infection and Hearing Loss
Identification of Predictive Markers for Testis Cancer in a Population of Men With High Risk
Salt Sensitivity Hypertension and Lens Opacities
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