Molecular characterization of two novel VEGFR3 mutations in Japanese families with Milroy's disease

Pediatr Int. 2008 Feb;50(1):116-8. doi: 10.1111/j.1442-200X.2007.02505.x.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Asian People / genetics
  • DNA, Complementary / analysis
  • Female
  • Humans
  • Infant
  • Infant, Newborn
  • Japan
  • Lymphedema / genetics*
  • Male
  • Mutation*
  • Mutation, Missense
  • Pedigree
  • Vascular Endothelial Growth Factor Receptor-3 / genetics*

Substances

  • DNA, Complementary
  • Vascular Endothelial Growth Factor Receptor-3