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Biomolecules | Free Full-Text | Functional Evaluation of a Rare Variant c.516G>C (p.Trp172Cys) in the GJB2 (Connexin 26) Gene Associated with Nonsyndromic Hearing Loss
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GJB2 molecular structure and localization. GJB2 gene is localized in... | Download Scientific Diagram
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Exome sequencing analysis reveals homozygous GJB2 gene mutation in a Mexican family with profound hearing loss | Revista Médica del Hospital General de México
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Analysis of the GJB2 Gene and its Mutated Protein in Non-Syndromic Hearing Loss Patients of Gilgit-Baltistan
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Frontiers | DFNB1 Non-syndromic Hearing Impairment: Diversity of Mutations and Associated Phenotypes
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Genes | Free Full-Text | High Rates of Three Common GJB2 Mutations c.516G>C, c.-23+1G>A, c.235delC in Deaf Patients from Southern Siberia Are Due to the Founder Effect
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Five-family pedigree. The graphic depicts GJB2 gene mutations (A-E).... | Download Scientific Diagram
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In Vitro Models of GJB2-Related Hearing Loss Recapitulate Ca2+ Transients via a Gap Junction Characteristic of Developing Cochlea - ScienceDirect
GBW09122 Plasmid DNA of deafness GJB2 gene reference material - National Sharing Platform for Reference Materials
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Analysis of the GJB2 Gene and its Mutated Protein in Non-Syndromic Hearing Loss Patients of Gilgit-Baltistan
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