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- W2890414287 abstract "Knobloch syndrome is a rare genetic disorder classically defined by a triad of occipital defect, high myopia, and vitreoretinal degeneration with high risk for retinal detachment. Our study aims to characterize the morphological changes of the retina in patients with Knobloch syndrome using optical coherence tomography (OCT)." @default.
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- W2890414287 date "2018-08-01" @default.
- W2890414287 modified "2023-09-27" @default.
- W2890414287 title "Optical coherence tomography in Knobloch syndrome" @default.
- W2890414287 doi "https://doi.org/10.1016/j.jaapos.2018.07.248" @default.
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