[Correction of CFTR anomalies: pharmacological approach]

Arch Pediatr. 2000 May:7 Suppl 2:352s-354s. doi: 10.1016/s0929-693x(00)80098-6.
[Article in French]
No abstract available

MeSH terms

  • Child
  • Chloride Channels / drug effects
  • Chloride Channels / genetics
  • Clinical Trials as Topic
  • Cystic Fibrosis / drug therapy*
  • Cystic Fibrosis Transmembrane Conductance Regulator / drug effects
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics*
  • DNA Mutational Analysis
  • Humans
  • Prognosis
  • Sodium Channels / drug effects
  • Sodium Channels / genetics

Substances

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