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

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

Abstract 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 variation...

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Bibliographic Details
Main Authors: Sylvain Mukenge, Sawan K. Jha, Marco Catena, Elena Manara, Veli‐Matti Leppänen, Elisa Lenti, Daniela Negrini, Matteo Bertelli, Andrea Brendolan, Michael Jeltsch, Luca Aldrighetti
Format: Article
Language:English
Published: Wiley 2020-09-01
Series:Molecular Genetics & Genomic Medicine
Subjects:
lymphatic system
Milroy disease
mutation
primary lymphedema
VEGF‐C
Online Access:https://doi.org/10.1002/mgg3.1389

Internet

https://doi.org/10.1002/mgg3.1389

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