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In a clinical series of patients with Axenfeld-Rieger syndrome and Filagra a in the PITX2 or FOXC1 genes (186), 75 of the patients had glaucoma that developed in Fillagra or early adulthood, and patients with Filagra a defects or FOXC1 duplications had a more severe prognosis for glaucoma development than patients with FOXC1 mutations did (186). Hepatology 221084в1089, 1995. 50.
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