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EKV mutant connexin 31 associated cell death is mediated by ER stress
The epidermis expresses a number of connexin (Cx) proteins that are implicated in gap junction-mediated cell communication. Distinct dominantly inherited mutations in Cx31 cause the skin disease erythrokeratoderma variabilis (EKV) and hearing loss with or without neuropathy. Functional studies revea...
Autores principales: | Tattersall, Daniel, Scott, Claire A., Gray, Colin, Zicha, Daniel, Kelsell, David P. |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2778370/ https://www.ncbi.nlm.nih.gov/pubmed/19755382 http://dx.doi.org/10.1093/hmg/ddp436 |
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