Lymphedema-distichiasis syndrome and FOXC2 gene mutation

SYSTEM OF OPHTHALMOLOGY

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The homeotic gene fork head encodes a nuclear protein and is expressed in the terminal regions of the Drosophila embryo

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Missense mutations interfere with VEGFR-3 signalling in primary lymphoedema

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Mutations in FOXC2 (MFH-1), a Forkhead Family Transcription Factor, Are Responsible for the Hereditary Lymphedema-Distichiasis Syndrome

Jianming Fang, Susan L. Dagenais, Robert P. Erickson et al. · The American Journal of Human Genetics · 2000 · 613 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10