Mutations in the VEGFR3 Signaling Pathway Explain 36% of Familial Lymphedema

Lymphedema is caused by dysfunction of lymphatic vessels, leading to disabling swelling that occurs mostly on the extremities. Lymphedema can be either primary (congenital) or secondary (acquired). Familial primary lymphedema commonly segregates in an autosomal dominant or recessive manner. It can a...

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Autors principals: Mendola, A., Schlögel, M.J., Ghalamkarpour, A., Irrthum, A., Nguyen, H.L., Fastré, E., Bygum, A., van der Vleuten, C., Fagerberg, C., Baselga, E., Quere, I., Mulliken, J.B., Boon, L.M., Brouillard, P., Vikkula, M.
Format: Artigo
Idioma:Inglês
Publicat: S. Karger AG 2013
Matèries:
Original Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3776465/
https://ncbi.nlm.nih.gov/pubmed/24167460
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000354097
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