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
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.
Gordon K et al.
Circulation Research, 2013
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