Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis

Cell. 1993 Jul 2;73(7):1251-4. doi: 10.1016/0092-8674(93)90353-r.
No abstract available

Publication types

  • Review

MeSH terms

  • Chloride Channels
  • Chlorides / metabolism*
  • Cystic Fibrosis / metabolism*
  • Cystic Fibrosis Transmembrane Conductance Regulator
  • Gene Deletion
  • Humans
  • Membrane Proteins / genetics*
  • Membrane Proteins / metabolism
  • Mutation
  • Phenotype
  • Protein Processing, Post-Translational

Substances

  • CFTR protein, human
  • Chloride Channels
  • Chlorides
  • Membrane Proteins
  • Cystic Fibrosis Transmembrane Conductance Regulator