Cystic fibrosis: a multiple exocrinopathy caused by dysfunctions in a multifunctional transport protein

Am J Med. 1998 Jun;104(6):576-90. doi: 10.1016/s0002-9343(98)00119-3.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Cystic Fibrosis / genetics
  • Cystic Fibrosis / metabolism*
  • Cystic Fibrosis / therapy
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics
  • Cystic Fibrosis Transmembrane Conductance Regulator / metabolism*
  • Epithelium / metabolism
  • Genetic Therapy
  • Humans
  • Mutation
  • Severity of Illness Index

Substances

  • CFTR protein, human
  • Cystic Fibrosis Transmembrane Conductance Regulator