PAX6 gene analysis in Serbian patients with aniridia
Introduction: Aniridia is a rare congenital eye anomaly associated with various ophthalmological problems. Some of the causes of this disease are mutations in the PAX6 gene or deletion of loci on the short arm of chromosome eleven, which can be complete or partial. In this study, PAX6 gene sequence...
| Main Authors: | , |
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| Format: | Article |
| Language: | English |
| Published: |
University of Belgrade, Medical Faculty
2016-01-01
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| Series: | Medicinski Podmladak |
| Subjects: | |
| Online Access: | http://scindeks-clanci.ceon.rs/data/pdf/0369-1527/2016/0369-15271601041C.pdf |