A novel complex insertion-deletion mutation in the FOXC2 gene in a Japanese patient with Lymphedema-Distichiasis Syndrome

Itoh M, Nakagawa H. A novel complex insertion-deletion mutation in the FOXC2 gene in a Japanese patient with Lymphedema-Distichiasis Syndrome. Eur J Dermatol. 2013 Jun 7. [Epub ahead of print].