A comprehensive CFTR mutation analysis of German cystic fibrosis patients

Hum Mol Genet. 1993 Jun;2(6):809-11. doi: 10.1093/hmg/2.6.809.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Base Sequence
  • Cystic Fibrosis / ethnology
  • Cystic Fibrosis / genetics*
  • Cystic Fibrosis Transmembrane Conductance Regulator
  • Germany / ethnology
  • Humans
  • Italy / ethnology
  • Membrane Proteins / genetics*
  • Molecular Sequence Data
  • Mutation*
  • Point Mutation
  • Spain / ethnology

Substances

  • CFTR protein, human
  • Membrane Proteins
  • Cystic Fibrosis Transmembrane Conductance Regulator