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<i>FOXC2</i> Disease Mutations Identified in Lymphedema Distichiasis Patients Impair Transcriptional Activity and Cell Proliferation
<i>FOXC2</i> is a member of the human forkhead-box gene family and encodes a regulatory transcription factor. Mutations in <i>FOXC2</i> have been associated with lymphedema distichiasis (LD), an autosomal dominant disorder that primarily affects the limbs. Most patients also...
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| 主要な著者: | , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
MDPI AG
2020-07-01
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| シリーズ: | International Journal of Molecular Sciences |
| 主題: | |
| オンライン･アクセス: | https://www.mdpi.com/1422-0067/21/14/5112 |
| タグ: |
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