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Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinase.

Bibliographic reference Irrthum, A ; Alitalo, Kari ; Karkkainen, M J ; Devriendt, Koenraad ; Vikkula, Miikka. Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinase.. In: American journal of human genetics, Vol. 67, no. 2, p. 295-301 (2000)
Permanent URL http://hdl.handle.net/2078.1/21963