Investigation on the role of biallelic variants in VEGF‐C found in a patient affected by Milroy‐like lymphedema

BACKGROUND: Milroy‐like disease is the diagnostic definition used for patients with phenotypes that resemble classic Milroy disease (MD) but are negative to genetic testing for FLT4. In this study, we aimed at performing a genetic characterization and biochemical analysis of VEGF‐C variations found...

Descripción completa

Detalles Bibliográficos
Autores principales: Mukenge, Sylvain, Jha, Sawan K., Catena, Marco, Manara, Elena, Leppänen, Veli‐Matti, Lenti, Elisa, Negrini, Daniela, Bertelli, Matteo, Brendolan, Andrea, Jeltsch, Michael, Aldrighetti, Luca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7507552/
https://www.ncbi.nlm.nih.gov/pubmed/32592340
http://dx.doi.org/10.1002/mgg3.1389

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7507552/
https://www.ncbi.nlm.nih.gov/pubmed/32592340
http://dx.doi.org/10.1002/mgg3.1389

Ejemplares similares