Splice-site mutations in VEGFC cause loss of function and Nonne-Milroy-like primary lymphedema.

Authors :: Fastré E
Lanteigne LE
Helaers R
Giacalone G
Revencu N
Dionyssiou D
Demiri E
Brouillard P
Vikkula M
Source :: Clinical genetics [Clin Genet] 2018 Jul; Vol. 94 (1), pp. 179-181. Date of Electronic Publication: 2018 Mar 15.
Publication Year :: 2018

Subjects :: DNA Mutational Analysis
Genetic Loci
Humans
Pedigree
Phenotype
Genetic Association Studies methods
Loss of Function Mutation
Lymphedema diagnosis
Lymphedema genetics
RNA Splice Sites
Vascular Endothelial Growth Factor C genetics

Full Text Access

Tools