Splice‐site mutations in VEGFC cause loss of function and Nonne‐Milroy‐like primary lymphedema. Issue 1 (15th March 2018)

• Record Type: Journal Article
• Authors: Fastré, E.; Lanteigne, L‐E.; Helaers, R.; Giacalone, G.; Revencu, N.; Dionyssiou, D.; Demiri, E.; Brouillard, P.; Vikkula, M.
• Is Part Of: Clinical genetics. Volume 94:Issue 1(2018)
• Page Start: 179
• Page End: 181
• Publication Date: 2018-03-15
• Subjects: lymphatic -- mutation -- primary lymphedema -- VEGFR3; Medical genetics -- Periodicals; 616.0420
• DOI: 10.1111/cge.13204
• Languages: English
• ISSNs: 0009-9163

Abstract

Abstract :