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Primary systemic carnitine deficiency Primary systemic carnitine deficiency is a rare, autosomal recessive disorder caused by mutations (including deletions) in the SLC22A5 gene coding for carnitine transporter protein OCTN2 (organic cation transporter novel 2) (33)
Case Overview Clinical studies and drug labeling from the U.S
The effects of glucose and insulin on renal electrolyte transport
Y.EisenbergY.FiresteinB
Heparan sulfate in perlecan promotes mouse atherosclerosis: roles in lipid permeability, lipid retention, and smooth muscle cell proliferation
He L, Feng D, Guo H, et al
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