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Browsing by Author Elbaz, U
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Title
Author(s)
Issue Date
A de novo mutation in PITX2 underlies a unique form of Axenfeld-Rieger syndrome with corneal neovascularization and extensive proliferative vitreoretinopathy
Journal:
Ophthalmic Genetics
Kletke, SN
Vincent, A
Maynes, JT
Elbaz, U
Mireskandari, K
Lam, WC
Ali, A
2020