The syndromic deafness mutation G12R impairs fast and slow gating in Cx26 hemichannels
{{output}}
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 proper... ...
