The syndromic deafness mutation G12R impairs fast and slow gating in Cx26 hemichannels

Mutations in connexin 26 (Cx26) hemichannels can lead to syndromic deafness that affects the cochlea and skin. These mutations lead to gain-of-function hemichannel phenotypes by unknown molecular mechanisms. In this study, we investigate the biophysical properties of the syndromic mutant Cx26G12R (G...

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Detalles Bibliográficos
Autores principales: García, Isaac E., Villanelo, Felipe, Contreras, Gustavo F., Pupo, Amaury, Pinto, Bernardo I., Contreras, Jorge E., Pérez-Acle, Tomás, Alvarez, Osvaldo, Latorre, Ramon, Martínez, Agustín D., González, Carlos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2018
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5940247/
https://www.ncbi.nlm.nih.gov/pubmed/29643172
http://dx.doi.org/10.1085/jgp.201711782

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5940247/
https://www.ncbi.nlm.nih.gov/pubmed/29643172
http://dx.doi.org/10.1085/jgp.201711782

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