Novel FOXC2 Mutation and Distichiasis in a Patient With Lymphedema-Distichiasis Syndrome
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Ophthalmology,General Medicine,Surgery
Reference11 articles.
1. Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome.;Fang;Am J Hum Genet,2000
2. A gene for lymphedema-distichiasis maps to 16q24.3.;Mangion;Am J Hum Genet,1999
3. Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24.;Brice;J Med Genet,2002
4. Truncating mutations in FOXC2 cause multiple lymphedema syndromes.;Finegold;Hum Mol Genet,2001
5. Phenotypic characterization of primary lymphedema.;Connell;Ann N Y Acad Sci,2008
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