A Missense Mutation of Mouse OCTN2, a Sodium-Dependent Carnitine Cotransporter, in the Juvenile Visceral Steatosis Mouse

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Biochemical and Biophysical Research Communications, Vol. 252, Iss. 3, 1998-11 ,pp. : 590-594

Elsevier

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Carnitine Uptake Defect: Frameshift Mutations in the Human Plasmalemmal Carnitine Transporter Gene

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GFP–Human High-Affinity Carnitine Transporter OCTN2 Protein: Subcellular Localization and Functional Restoration of Carnitine Uptake in Mutant Cell Lines with the Carnitine Transporter Defect

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Carnitine Palmitoyltransferase I Activity Monitoring in Fibroblasts and Leukocytes Using Electrospray Ionization Mass Spectrometry

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