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Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratoderma

Developmental BiologyMendelian DisorderGenetic DisorderGeneticsFunctional DefectsCraniofacial DevelopmentDominant Deaf-mutismMolecular GeneticsDermatologyMedicinePalmoplantar Keratoderma