Two common mutations 934C to G and 937C to G of fibroblast growth factor receptor 2 (FGFR2) gene in Chinese patients with Apert syndrome

Hum Mutat. 1998:Suppl 1:S18-9. doi: 10.1002/humu.1380110106.
No abstract available

MeSH terms

  • Acrocephalosyndactylia / genetics*
  • Amino Acid Substitution
  • China / ethnology
  • DNA / chemistry
  • DNA / genetics
  • DNA / metabolism
  • DNA Mutational Analysis
  • Deoxyribonucleases, Type II Site-Specific / metabolism
  • Humans
  • Point Mutation
  • Receptor Protein-Tyrosine Kinases / genetics*
  • Receptor, Fibroblast Growth Factor, Type 2
  • Receptors, Fibroblast Growth Factor / genetics*
  • Taiwan

Substances

  • Receptors, Fibroblast Growth Factor
  • DNA
  • FGFR2 protein, human
  • Receptor Protein-Tyrosine Kinases
  • Receptor, Fibroblast Growth Factor, Type 2
  • endodeoxyribonuclease SfiI
  • CGCG-specific type II deoxyribonucleases
  • Deoxyribonucleases, Type II Site-Specific