Primary non-syndromic lymphoedema (Meige disease) is not caused by mutations in FOXC2-Reference-Cited by-同舟云学术

Primary non-syndromic lymphoedema (Meige disease) is not caused by mutations in FOXC2

Published:2008-01-16 Issue:3 Volume:16 Page:300-304
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Rezaie Tayebeh,Ghoroghchian Rose,Bell Rachel,Brice Glen,Hasan Ali,Burnand Kevin,Vernon Steve,Mansour Sahar,Mortimer Peter,Jeffery Steve,Child Anne,Sarfarazi Mansoor

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/5201982.pdf

Reference17 articles.

1. Brice G, Mansour S, Bell R et al: Analysis of the phenotypic abnormalities in lymphoedema–distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24. J Med Genet 2002; 39: 478–483.

2. Mellor R, Brice G, Stanton A et al: Mutations in FOXC2 are strongly associated with primary valve failure in veins of the lower limb. Circulation 2007; 115: 1912–1920.

3. Evans AL, Brice G, Sotirova V et al: Mapping of primary congenital lymphedema to the 5q35.3 region. Am J Hum Genet 1999; 64: 547–555.

4. Ferrell RE, Levinson KL, Esman JH et al: Hereditary lymphedema: evidence for linkage and genetic heterogeneity. Hum Mol Genet 1998; 7: 2073–2078.

5. Mangion J, Rahman N, Mansour S et al: A gene for lymphedema–distichiasis maps to 16q24.3. Am J Hum Genet 1999; 65: 427–432.

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