A Mutation in VEGFC, a Ligand for VEGFR3, is Associated with Autosomal Dominant Milroy-like Primary Lymphedema

@inproceedings{Gordon2013AMI,
  title={A Mutation in VEGFC, a Ligand for VEGFR3, is Associated with Autosomal Dominant Milroy-like Primary Lymphedema},
  author={Kristiana D. Gordon and D{\"o}rte Schulte and Glen Brice and Michael J. A. Simpson and Guy M. Roukens and Andreas van Impel and Fiona Connell and Kamini Kalidas and Steve Jeffery and Peter Mortimer and Sahar Mansour and Stefan Schulte-Merker and Pia Ostergaard},
  year={2013}
}
Department of Clinical Sciences, St George's University of London, London SW17 0RE, UK; Hubrecht Institute, KNAW – UMC Utrecht, 3584 CT Utrecht, Netherland; Thames Regional Genetics Service, St. George's University of London, London SW17 0RE, UK; Division of Genetics and Molecular Medicine, King’s College London School of Medicine, Guy’s Hospital, London SE1 9RT, UK; Clinical Genetics, Guy's and St Thomas' NHS Foundation Trust, Guy's Hospital, London SE1 9RT, UK; Human Genetics Research Centre… CONTINUE READING