Mutations in the VEGFR3 Signaling Pathway Explain 36% of Familial Lymphedema-Reference-Cited by-同舟云学术

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

Published:2013 Issue:6 Volume:4 Page:257-266
ISSN:1661-8769
Container-title:Molecular Syndromology
language:en
Short-container-title:Mol Syndromol

Author:

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.,

Publisher

S. Karger AG

Subject

Genetics (clinical),Genetics

Cited by 89 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Lymphedema vs lipedema: Similar but different;Cleveland Clinic Journal of Medicine;2024-07

2. Disorders Affecting Cutaneous Vasculature;Rook's Textbook of Dermatology;2024-03-19

3. VEGFR-3 signaling in macrophages: friend or foe in disease?;Frontiers in Immunology;2024-02-22

4. The role of key biomarkers in lymphatic malformation: An updated review;The Journal of Gene Medicine;2024-02

5. PKD1L1 Is Involved in Congenital Chylothorax;Cells;2024-01-12

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