Is the spectrum of mutations in Indian patients with cystic fibrosis different?

Am J Med Genet. 2000 Jul 17;93(2):161-3. doi: 10.1002/1096-8628(20000717)93:2<161::aid-ajmg15>3.0.co;2-l.
No abstract available

Publication types

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

MeSH terms

  • Adult
  • Alternative Splicing / genetics
  • Amino Acid Substitution
  • Base Sequence
  • Child
  • Child, Preschool
  • Cystic Fibrosis / genetics*
  • Cystic Fibrosis / pathology
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics*
  • DNA / chemistry
  • DNA / genetics
  • DNA Mutational Analysis
  • Female
  • Humans
  • India
  • Infant
  • Infant, Newborn
  • Male
  • Mutagenesis, Insertional
  • Mutation
  • Point Mutation
  • Polymorphism, Single-Stranded Conformational

Substances

  • CFTR protein, human
  • cystic fibrosis transmembrane conductance regulator delta F508
  • Cystic Fibrosis Transmembrane Conductance Regulator
  • DNA