| 1 | FOXC1, IRID1 |
| Severe molecular defects of a novel FOXC1 W152G mutation result in aniridia. | |
| Ito YA, Footz TK, Berry FB, Mirzayans F, Yu M, Khan AO, Walter MA. | |
| Invest Ophthalmol Vis Sci. 50(8):3573-9. 2009 | |
| 2 | ASMD2, ASMD3, ASMD4, ASMD5, ASMFD, AXR1, AXR2, FOXC1, IRID1, MAF, PAX6, PITX2, RIEG1, RIEG2 |
| Molecular and developmental mechanisms of anterior segment dysgenesis. | |
| Sowden JC. | |
| Eye 21(10):1310-8. Review. 2007 | |