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

Splice-site mutations in VEGFC cause loss of function and Nonne-Milroy-like primary lymphedema. Clin Genet. 2018 Mar 15;: Authors: Fastré E, Lanteigne LE, Helaers R, Giacalone G, Revencu N, Dionyssiou D, Demiri E, Brouillard P, Vikkula M PMID: 29542815 [PubMed - as supplied by publisher]

https://www.ncbi.nlm.nih.gov/pubmed/29542815?dopt=Abstract

Source: Clinical Genetics - March 15, 2018 Category: Genetics & Stem Cells Authors: Fastré E, Lanteigne LE, Helaers R, Giacalone G, Revencu N, Dionyssiou D, Demiri E, Brouillard P, Vikkula M Tags: Clin Genet Source Type: research

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