Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome

• FANG J

収録刊行物

• Am J Hum Genet

  Am J Hum Genet 67 1382-1388, 2000

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• CRID: 1570291225643803904
• NII論文ID: 10021998515
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