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Tyni T, Kivela T, Lappi M, Summanen P, Nikoskelainen E, Pihko H: Ophthalmologic findings in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation: a new type of hereditary metabolic chorioretinopathy
Luxury mountain living meets unbeatable convenience in this beautifully remodeled 2-bedroom, 2-bath condo at Mt
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