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Mutations in Connexin-31 (Cx31) are associated with multiple human diseases including erythrokeratodermia variabilis (EKV). The… Expand Hearing impairment (HI) affects 1/1000 children and over 2% of the aged population. We have previously reported that mutations in… Expand A 51-year-old woman presented with well-demarcated, erythematous patches and hyperkeratotic plaques that were arranged… Expand Erythrokeratodermia variabilis is an autosomal dominant genodermatosis characterized by persistent plaque-like or generalized… Expand Communication and interaction between cells has been shown to be important during the embryonic development of the vertebrate… Expand The connexin31 (Cx31) gene, a member of the connexin multigene family, is expressed in a characteristic spatiotemporal pattern… Expand Mutations in the GJB3 gene encoding connexin31 (Cx31) can cause a dominant non-syndromic form of hearing loss (DFNA2). To… Expand factors1. Mutations in the connexin26 gene (GJB2), located on 13q12, are responsible for non-syndromic recessive and dominant… Expand Abstract During segmentation of the mouse hindbrain (d8.0–8.5 pc), expression of the gap junction gene connexin31 (cx31) is… Expand A new member of the connexin gene family has been identified and designated rat connexin-31 (Cx31) based on its predicted… Expand