Congenital Hereditary Lymphedema Caused by a Mutation That Inactivates VEGFR3 Tyrosine Kinase
- 1 August 2000
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 67 (2) , 295-301
- https://doi.org/10.1086/303019
Abstract
No abstract availableKeywords
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