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Eye anomalies and neurological manifestations in patients with PAX6 mutations
Molecular Vision, 10/26/09
Chien YH et al. – Both novel and known PAX6 mutations were identified in the current study, and PAX6 mutations were closely associated with aniridia. Absence of a positive family history does not exclude PAX6 mutation. The frequent occurrence of developmental delay in patients with PAX6 mutation argues for a prompt diagnosis of the disease.
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A 1-Year Retrospective Review of Ranibizumab for Naive Nonsubfoveal Choroidal Neovascularization Secondary To Age-Related Macular Degeneration
Retina, 11/25/09
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