Functional characterization of a novel Cx26 (T55N) mutation associated to non-syndromic hearing loss

This publication has 26 references indexed in Scilit:

• Loss‐of‐function and residual channel activity of connexin26 mutations associated with non‐syndromic deafness
  FEBS Letters, 2002
• Functional Analysis of a Dominant Mutation of Human Connexin26 Associated with Nonsyndromic Deafness
  Cell Communication & Adhesion, 2001
• Functional analysis of human Cx26 mutations associated with deafness
  Published by Elsevier ,2000
• Connexin26 mutations associated with the most common form of non- syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans
  Human Molecular Genetics, 1997
• Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
  Nature, 1997
• Genes responsible for human hereditary deafness: symphony of a thousand
  Nature Genetics, 1996
• Connections with Connexins: the Molecular Basis of Direct Intercellular Signaling
  European Journal of Biochemistry, 1996
• Specific permeability and selective formation of gap junction channels in connexin-transfected HeLa cells.
  The Journal of cell biology, 1995
• Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis
  Brain Structure and Function, 1995
• Selective dye and ionic permeability of gap junction channels formed by connexin45.
  Circulation Research, 1994