Cystic fibrosis mutations in heterozygous newborns with hypertrypsinemia and low sweat chloride

Am J Hum Genet. 1999 Jan;64(1):303-4. doi: 10.1086/302212.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chlorides / analysis*
  • Cystic Fibrosis / genetics*
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics
  • Heterozygote
  • Humans
  • Infant, Newborn
  • Mutation*
  • Sweat / chemistry*
  • Trypsin / blood*

Substances

  • CFTR protein, human
  • Chlorides
  • Cystic Fibrosis Transmembrane Conductance Regulator
  • Trypsin