First study of the F508del mutation in Malaysian children diagnosed with cystic fibrosis

J Paediatr Child Health. 2011 Aug;47(8):573-5. doi: 10.1111/j.1440-1754.2011.02149.x.
No abstract available

Publication types

  • Letter

MeSH terms

  • Child
  • Child, Preschool
  • Consanguinity
  • Cystic Fibrosis / diagnosis
  • Cystic Fibrosis / genetics*
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics*
  • DNA Primers
  • Female
  • Genotype
  • Humans
  • Infant
  • Malaysia
  • Male
  • Mutation
  • Retrospective Studies
  • Sequence Deletion

Substances

  • CFTR protein, human
  • DNA Primers
  • Cystic Fibrosis Transmembrane Conductance Regulator