Citations for
1CAASDS, VSX1
VSX1 (RINX) mutation with craniofacial anomalies, empty sella, corneal endothelial changes, and abnormal retinal and auditory bipolar cells.
Mintz-Hittner HA, Semina EV, Frishman LJ, Prager TC, Murray JC.
Ophthalmology 111(4):828-36. 2004