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Screening for Mutations of Axenfeld-Rieger Syndrome Caused by FOXC1Gene in Japanese Patients
- Source :
- Journal of Glaucoma; December 2001, Vol. 10 Issue: 6 p477-482, 6p
- Publication Year :
- 2001
-
Abstract
- Mutations in the forkhead transcription factor gene (FOXC1) have been recently shown to cause some cases of juvenile glaucoma associated with a variety of anterior-segment anomalies. The purpose of this study was to investigate the clinical features of Axenfeld-Rieger syndrome caused by FOXC1mutations in Japanese patients.
Details
- Language :
- English
- ISSN :
- 10570829 and 1536481X
- Volume :
- 10
- Issue :
- 6
- Database :
- Supplemental Index
- Journal :
- Journal of Glaucoma
- Publication Type :
- Periodical
- Accession number :
- ejs49394453