A Novel Splice-Site Mutation in VEGFC Is Associated with Congenital Primary Lymphoedema of Gordon

Lymphedema is characterized by chronic swelling of any body part caused by malfunctioning or obstruction in the lymphatic system. Primary lymphedema is often considered genetic in origin. VEGFC, which is a gene encoding the ligand for the vascular endothelial growth factor receptor 3 (VEGFR3/FLT4) a...

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Detalles Bibliográficos
Autores principales: Nadarajah, Noeline, Schulte, Dörte, McConnell, Vivienne, Martin-Almedina, Silvia, Karapouliou, Christina, Mortimer, Peter S., Jeffery, Steve, Schulte-Merker, Stefan, Gordon, Kristiana, Mansour, Sahar, Ostergaard, Pia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6121331/
https://www.ncbi.nlm.nih.gov/pubmed/30071673
http://dx.doi.org/10.3390/ijms19082259

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6121331/
https://www.ncbi.nlm.nih.gov/pubmed/30071673
http://dx.doi.org/10.3390/ijms19082259

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