Mutations in the VEGFR3 signaling pathway explain 36% of familial lymphedema.

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Publication year
2013
Author(s)
Mendola, A.
Schlogel, M.J.
Ghalamkarpour, A.
Irrthum, A.
Nguyen, H.L.
Fastre, E.
Bygum, A.
Vleuten, C.J. van der
Fagerberg, C.
Baselga, E.
Quere, I.
Mulliken, J.B.
Boon, L.M.
Brouillard, P.
Vikkula, M.
Group, T.L.R.
Source
Molecular Syndromology, 4, 6, (2013), pp. 257-266
ISSN
Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/125693   https://hdl.handle.net/2066/125693
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