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bibliographicCitation Finegold DN, Kimak MA, Lawrence EC, Levinson KL, Cherniske EM, Pober BR, Dunlap JW, Ferrell RE. Truncating mutations in FOXC2 cause multiple lymphedema syndromes. Hum Mol Genet. 2001 May 15;10(11):1185–9. doi: 10.1093/hmg/10.11.1185. PMID: 11371511.
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title Truncating mutations in FOXC2 cause multiple lymphedema syndromes
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