You are here

Article info

Article menu

This article has a correction. Please see:

Download PDFPDF
New loci
Short report
A novel stop mutation in the vascular endothelial growth factor-C gene (VEGFC) results in Milroy-like disease

Authors

  • Emilia Balboa-Beltran Fundación Pública Galega de Medicina Xenómica, SERGAS, Santiago de Compostela, Spain PubMed articlesGoogle scholar articles
  • María J Fernández-Seara Servicio de Neonatología, Departamento de Pediatría, Hospital Clínico Universitario de Santiago de Compostela, Santiago de Compostela, Spain PubMed articlesGoogle scholar articles
  • Alejandro Pérez-Muñuzuri Servicio de Neonatología, Departamento de Pediatría, Hospital Clínico Universitario de Santiago de Compostela, Santiago de Compostela, Spain PubMed articlesGoogle scholar articles
  • Ramón Lago Fundación Pública Galega de Medicina Xenómica, SERGAS, Santiago de Compostela, Spain PubMed articlesGoogle scholar articles
  • Carlos García-Magán Servicio de Neonatología, Departamento de Pediatría, Hospital Clínico Universitario de Santiago de Compostela, Santiago de Compostela, Spain PubMed articlesGoogle scholar articles
  • María L Couce Servicio de Neonatología, Departamento de Pediatría, Hospital Clínico Universitario de Santiago de Compostela, Santiago de Compostela, Spain PubMed articlesGoogle scholar articles
  • Beatriz Sobrino Grupo de Medicina Xenómica-USC, CIBERER, Fundación Pública Galega de Medicina Xenómica, Santiago de Compostela, Spain PubMed articlesGoogle scholar articles
  • Jorge Amigo Grupo de Medicina Xenómica-USC, CIBERER, Fundación Pública Galega de Medicina Xenómica, Santiago de Compostela, Spain PubMed articlesGoogle scholar articles
  • Angel Carracedo Fundación Pública Galega de Medicina Xenómica, SERGAS, Santiago de Compostela, Spain Grupo de Medicina Xenómica-USC, CIBERER, Fundación Pública Galega de Medicina Xenómica, Santiago de Compostela, Spain King Abdulaziz University, Center of Excellence in Genomic Medicine Research, Jeddah, Saudi Arabia PubMed articlesGoogle scholar articles
  • Francisco Barros Fundación Pública Galega de Medicina Xenómica, SERGAS, Santiago de Compostela, Spain Grupo de Medicina Xenómica-USC, CIBERER, Fundación Pública Galega de Medicina Xenómica, Santiago de Compostela, Spain PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Francisco Barros, Fundación Pública Galega de Medicina Xenómica, Edf. Consultas planta-2, Hospital Clinico Universitario, Santiago de Compostela 15707, Spain; francisco.barros{at}usc.es
View Full Text

Citation

Balboa-Beltran E, Fernández-Seara MJ, Pérez-Muñuzuri A, et al
A novel stop mutation in the vascular endothelial growth factor-C gene (VEGFC) results in Milroy-like disease
Journal of Medical Genetics 2014;51:475-478.

Publication history

  • Received August 27, 2013
  • Revised March 9, 2014
  • Accepted March 26, 2014
  • First published April 17, 2014.
Online issue publication 
April 27, 2016

Article Versions

Request permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

Copyright information

Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions