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Ophthalmologic findings in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation: a new type of hereditary metabolic chorioretinopathy

Geissner A, Anish C, Seeberger PH

L- : : - 100 - 60 4000 - L- 1905

doi: 10.3390/nu13124433, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar] 72.Askari G, Nasiri M, Mozaffari-Khosravi H, Rezaie M, Bagheri-Bidakhavidi M, Sadeghi O
