A commentary on the novel complex allele [A238V;F508del] of the CFTR gene: clinical phenotype and possible implications for cystic fibrosis etiological therapies

J Hum Genet. 2016 Jun;61(6):471-2. doi: 10.1038/jhg.2016.34. Epub 2016 Apr 21.
No abstract available

Publication types

  • Letter

MeSH terms

  • Alleles*
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics
  • Cystic Fibrosis*
  • Humans
  • Mutation
  • Phenotype

Substances

  • Cystic Fibrosis Transmembrane Conductance Regulator