Missense variation of the CFTR gene codon 507

Hum Mutat. 1992;1(2):165. doi: 10.1002/humu.1380010213.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Codon / genetics
  • Cystic Fibrosis / genetics*
  • Cystic Fibrosis Transmembrane Conductance Regulator
  • Genetic Variation*
  • Homozygote
  • Humans
  • Membrane Proteins / genetics*

Substances

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