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    • Journal article
    Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinase.
    Irrthum, A Alitalo, Kari Karkkainen, M J Devriendt, Koenraad[UCL] Vikkula, Miikka[UCL] (2000) American journal of human genetics — Vol. 67, no. 2, p. 295-301 (2000)