Combination of ENaC and CFTR mutations may predispose to cystic fibrosis-like disease

Eur Respir J. 2009 Sep;34(3):772-3. doi: 10.1183/09031936.00057309.
No abstract available

Publication types

  • Letter

MeSH terms

  • Aged
  • Bronchiectasis / genetics*
  • Bronchiectasis / pathology*
  • Case-Control Studies
  • Cohort Studies
  • Cystic Fibrosis / genetics*
  • Cystic Fibrosis / pathology
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics*
  • Epithelial Sodium Channels / genetics*
  • Female
  • Humans
  • Male
  • Middle Aged
  • Mutation, Missense / genetics*

Substances

  • CFTR protein, human
  • Epithelial Sodium Channels
  • Cystic Fibrosis Transmembrane Conductance Regulator