Associated Papers
A Novel Splice-Site Mutation in VEGFC Is Associated with Congenital Primary Lymphoedema of Gordon.
Nadarajah N et al.
International Journal of Molecular Sciences, 2018
Splice-site mutations in VEGFC cause loss of function and Nonne-Milroy-like primary lymphedema.
Fastré E et al.
Clinical Genetics, 2018
A novel stop mutation in the vascular endothelial growth factor-C gene (VEGFC) results in Milroy-like disease.
Balboa-Beltran E et al.
Journal of Medical Genetics, 2014
Select a paper to view details