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Pediatr Int. 2008 Feb;50(1):116-8. doi: 10.1111/j.1442-200X.2007.02505.x.

Molecular characterization of two novel VEGFR3 mutations in Japanese families with Milroy's disease.

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Department of Pediatrics, Faculty of Medicine, University of Toyama, Toyama, Japan. futatani@tch.pref.toyama.jp
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