Splice-site mutations in VEGFC cause loss of function and Nonne-Milroy-like primary lymphedema

被引：18

作者：

Fastre, E. ^{[1
]}

Lanteigne, L-E. ^{[1
]}

Helaers, R. ^{[1
]}

Giacalone, G. ^{[2
]}

Revencu, N. ^{[3
]}

Dionyssiou, D. ^{[4
]}

Demiri, E. ^{[4
]}

Brouillard, P. ^{[1
]}

Vikkula, M. ^{[1
,5
]}

机构：

[1] Univ Louvain, de Duve Inst, Human Mol Genet, Ave Hippocrate 74,Bp 75-39, B-1200 Brussels, Belgium

[2] AZ Sint Maarten, Lymfectr, Mechelen, Belgium

[3] Univ Louvain, Clin Univ St Luc, Ctr Human Genet, Brussels, Belgium

[4] Aristotle Univ Thessaloniki, Papageorgiou Hosp, Dept Plast Surg, Thessaloniki, Greece

[5] Univ Louvain, WELB, Bussels, Belgium

来源：

关键词：

lymphatic; mutation; primary lymphedema; VEGFR3; GROWTH FACTOR-C;

D O I：

10.1111/cge.13204

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：179 / 181

页数：3

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