Wide clinical spectrum in a family with hereditary lymphedema type I due to a novel missense mutation in VEGFR3
2006; Springer Nature; Volume: 51; Issue: 10 Linguagem: Inglês
10.1007/s10038-006-0031-3
ISSN1435-232X
AutoresRonen Spiegel, Arash Ghalamkarpour, Etty Daniel‐Spiegel, Miikka Vikkula, Stavit A. Shalev,
Tópico(s)Sympathectomy and Hyperhidrosis Treatments
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