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Description
A lipidomic view of SARS-CoV-2

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Academic J.Shanghai Second Med.Univ

Hyperlysinemia, saccharopinuria, and 2-aminoadipic and 2-oxoadipic aciduria are generally considered benign disorders [27,34]: Glutaric aciduria type 1 is a rare autosomal recessive disease caused by glutaryl-CoA dehydrogenase deficiency

Ketone bodies can be cleared by the kidneys or lungs, converted into lipids, or transported to extrahepatic tissues for utilization

369 HoldenSMaksoudREaton-FitchNCabanasHStainesDMarshall-GradisnikS
