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28. Ophthalmologic findings in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation: a new type of hereditary metabolic chorioretinopathy. Tyni T; Kivelä T; Lappi M; Summanen P; Nikoskelainen E; Pihko H Ophthalmology; 1998 May; 105(5):810-24. PubMed ID: 9593380 [TBL] [Abstract][Full Text] [Related]
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30. Spinal fluid pleocytosis in acute posterior multifocal placoid pigment epitheliopathy. Fishman GA; Baskin M; Jednock N Ann Ophthalmol; 1977 Jan; 9(1):36-6. PubMed ID: 835959 [TBL] [Abstract][Full Text] [Related]
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