The establishment of a predictive mutational model of the forkhead domain through the analyses of FOXC2 missense mutations identified in patients with hereditary lymphedema with distichiasis.

Source:http://linkedlifedata.com/resource/pubmed/id/16081467

Hum. Mol. Genet. 2005 Sep 15 14 18 2619-27

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PMID
16081467