VSX1 (RINX) mutation with craniofacial anomalies, empty sella, corneal endothelial changes, and abnormal retinal and auditory bipolar cells

Helen A. Mintz-Hittner, Elena V. Semina, Laura J. Frishman, Thomas C. Prager, Jeffrey C. Murray

Research output: Contribution to journalArticlepeer-review

40 Scopus citations

Fingerprint

Dive into the research topics of 'VSX1 (RINX) mutation with craniofacial anomalies, empty sella, corneal endothelial changes, and abnormal retinal and auditory bipolar cells'. Together they form a unique fingerprint.

Medicine & Life Sciences