VSX1 (RINX) mutation with craniofacial anomalies, empty sella, corneal endothelial changes, and abnormal retinal and auditory bipolar cells*1
- 1 April 2004
- journal article
- Published by Elsevier in Ophthalmology
- Vol. 111 (4) , 828-836
- https://doi.org/10.1016/j.ophtha.2003.07.006
Abstract
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