Three children with Milroy disease and de novo mutations in VEGFR3

Clin Genet. 2007 Feb;71(2):187-9. doi: 10.1111/j.1399-0004.2007.00741.x.
No abstract available

Publication types

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

MeSH terms

  • Amino Acid Substitution
  • Child, Preschool
  • Female
  • Humans
  • Infant
  • Lymphedema / diagnosis
  • Lymphedema / genetics*
  • Male
  • Mutation*
  • Phenotype
  • Vascular Endothelial Growth Factor Receptor-3 / chemistry
  • Vascular Endothelial Growth Factor Receptor-3 / genetics*

Substances

  • Vascular Endothelial Growth Factor Receptor-3