Assessment of CFTR function in native epithelia for the diagnosis of cystic fibrosis

Pediatr Pulmonol Suppl. 2004:26:243. doi: 10.1002/ppul.70118.
No abstract available

MeSH terms

  • Cystic Fibrosis / diagnosis*
  • Cystic Fibrosis / genetics*
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics*
  • Genetic Testing*
  • Genotype
  • Humans
  • Mutation

Substances

  • CFTR protein, human
  • Cystic Fibrosis Transmembrane Conductance Regulator