FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome. Autor Kriederman, B, Myloyde, T, Witte, M, Dagenais, S, Witte, C, Rennels, M, Bernas, M, Lynch, M, Erickson, R, Caulder, MS, Miura, N, Jackson, D, Brooks, B, Glover, T