Cystic fibrosis diagnosis: new dilemmas for an old disorder

Pediatr Pulmonol. 2002 Feb;33(2):83-4. doi: 10.1002/ppul.10053.
No abstract available

Publication types

  • Comment
  • Editorial

MeSH terms

  • Codon, Nonsense
  • Cystic Fibrosis / diagnosis*
  • Cystic Fibrosis / genetics
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics
  • Cystic Fibrosis Transmembrane Conductance Regulator / metabolism*
  • Diagnosis, Differential
  • Humans
  • Mutation
  • Phenotype
  • Sweat / chemistry

Substances

  • CFTR protein, human
  • Codon, Nonsense
  • Cystic Fibrosis Transmembrane Conductance Regulator