Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinase.
Am J Hum Genet. 2000 Aug;67(2):295-301. doi: 10.1086/303019. Epub 2000 Jun 9.
Am J Hum Genet. 2000.
PMID: 10856194
Free PMC article.