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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...
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 |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
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 |
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