Molecular analysis of FOXC1 in subjects presenting with severe developmental eye anomalies.
PURPOSE: Haploinsufficiency through mutation or deletion of the forkhead transcription factor, FOXC1, causes Axenfeld-Rieger anomaly, which manifests as a range of anterior segment eye defects and glaucoma. The aim of this study is to establish whether mutation of FOXC1 contributes toward other dev...
| Main Authors: | , , |
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| Format: | Journal article |
| Language: | English |
| Published: |
2009
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