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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
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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

Publication history

  • Received August 27, 2013
  • Revised March 9, 2014
  • Accepted March 26, 2014
  • First published April 17, 2014.
Online issue publication 
June 13, 2014

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