|
|||||
|
|
Splice‐site mutations in VEGFC cause loss of function and Nonne‐Milroy‐like primary lymphedema |
|
| Authors: | E. Fastré L‐E. Lanteigne R. Helaers G. Giacalone N. Revencu D. Dionyssiou E. Demiri P. Brouillard M. Vikkula |
| Affiliation: | 1. Human Molecular Genetics, de Duve Institute, University of Louvain, Brussels, Belgium;2. Lymfecentrum, AZ Sint‐Maarten, Mechelen, Belgium;3. Center for Human Genetics, Cliniques universitaires Saint‐Luc, University of Louvain, Brussels, Belgium;4. Department of Plastic Surgery, Papageorgiou Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece;5. Walloon Excellence in Lifesciences and Biotechnology (WELBIO), University of Louvain, Bussels, Belgium |
| Abstract: | |
| Keywords: | lymphatic mutation primary lymphedema VEGFR3 |