Mutation in Vascular Endothelial Growth Factor-C, a Ligand for Vascular Endothelial Growth Factor Receptor-3, Is Associated With Autosomal Dominant Milroy-Like Primary Lymphedema-Reference-Cited by-同舟云学术

Mutation in Vascular Endothelial Growth Factor-C, a Ligand for Vascular Endothelial Growth Factor Receptor-3, Is Associated With Autosomal Dominant Milroy-Like Primary Lymphedema

Published:2013-03-15 Issue:6 Volume:112 Page:956-960
ISSN:0009-7330
Container-title:Circulation Research
language:en
Short-container-title:Circ Res

Author:

Gordon Kristiana¹,Schulte Dörte¹,Brice Glen¹,Simpson Michael A.¹,Roukens M. Guy¹,van Impel Andreas¹,Connell Fiona¹,Kalidas Kamini¹,Jeffery Steve¹,Mortimer Peter S.¹,Mansour Sahar¹,Schulte-Merker Stefan¹,Ostergaard Pia¹

Affiliation:

1. From the Department of Clinical Sciences, St George’s University of London, London, United Kingdom (K.G., P.S.M.); Hubrecht Institute, KNAW- UMC Utrecht, the Netherlands (D.S., M.G.R., A.v.I., S.S-M.); SW Thames Regional Genetics Service, St. George’s Healthcare NHS Trust, London, United Kingdom (G.B., S.M.); Division of Genetics and Molecular Medicine, King’s College London School of Medicine, Guy’s Hospital, London, United Kingdom (M.A.S.); Clinical Genetics, Guy’s and St Thomas’ NHS Foundation...

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine,Physiology

Reference9 articles.

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3. Analysis of the coding regions of VEGFR3 and VEGFC in Milroy disease and other primary lymphoedemas

4. FLT4/VEGFR3and Milroy Disease: Novel Mutations, a Review of Published Variants and Database Update

5. ccbe1 is required for embryonic lymphangiogenesis and venous sprouting

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