Drowning out communication. Focus on "The human Cx26-D50A and Cx26-A88V mutations causing keratitis-ichthyosis-deafness syndrome display increased hemichannel activity"

Am J Physiol Cell Physiol. 2013 Jun 15;304(12):C1129-30. doi: 10.1152/ajpcell.00087.2013. Epub 2013 Apr 10.
No abstract available

Publication types

  • Editorial
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Comment

MeSH terms

  • Animals
  • Connexin 26
  • Connexins / genetics*
  • Deafness / genetics*
  • Female
  • Humans
  • Ichthyosis / genetics*
  • Keratitis / genetics*
  • Mutation / genetics*

Substances

  • Connexins
  • GJB2 protein, human
  • Connexin 26

Supplementary concepts

  • Keratitis, Ichthyosis, and Deafness (KID) Syndrome