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

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43 Scopus citations

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Medicine and Dentistry

Biochemistry, Genetics and Molecular Biology