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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

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