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Description
Ophthalmologic findings in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation: a new type of hereditary metabolic chorioretinopathy
doi: 10.7759/cureus.1898
PMID: 33084011
doi: 10.1016/j.mce.2011.08.008 8 HaradaNHanadaKMinamiYKitakazeTOgataYTokumotoHet al
