Truncating mutations in FOXC2 cause multiple lymphedema syndromes.
Finegold DN; Kimak MA; Lawrence EC; Levinson KL; Cherniske EM; Pober BR; Dunlap JW; Ferrell RE; Human Molecular Genetics, 2001, vol. 10, issue 11, p 1185, ISSN 09646906. ISBN 09646906.

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