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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書誌詳細
主要な著者: 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.
フォーマット: Artigo
言語:Inglês
出版事項: S. Karger AG 2013
主題:
Original Article
オンライン･アクセス: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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