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Wide clinical spectrum in a family with hereditary lymphedema type I due to a novel missense mutation inVEGFR3

โœ Scribed by Ronen Spiegel; Arash Ghalamkarpour; Etty Daniel-Spiegel; Miikka Vikkula; Stavit A Shalev


Publisher
Nature Publishing Group
Year
2006
Tongue
English
Weight
163 KB
Volume
51
Category
Article
ISSN
1435-232X

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