FLT4 Mutations Are Associated with Segmental Lymphatic Dysfunction and Initial Lymphatic Aplasia in Patients with Milroy Disease

This study explored mutations in the Fms-related tyrosine kinase 4/vascular endothelial growth factor receptor 3 gene (FLT4) and lymphatic defects in patients with Milroy disease (MD). Twenty-nine patients with lower limb lymphedema were enrolled. Sixteen patients had a familial history of MD, while...

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Detalles Bibliográficos
Autores principales: Liu, Ningfei, Gao, Minzhe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8535675/
https://www.ncbi.nlm.nih.gov/pubmed/34681005
http://dx.doi.org/10.3390/genes12101611

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8535675/
https://www.ncbi.nlm.nih.gov/pubmed/34681005
http://dx.doi.org/10.3390/genes12101611

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