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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

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The current results showed that the levels of those cations were dramatically reduced in TMX-treated rats

CSB-E08364r) were estimated in the brain by using commercial rat ELISA kits obtained from Cloud-Clone Crop, Eagle Biosciences Inc, and Cusabio (USA), respectively
