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Human Molecular Genetics|March 11, 1999
Mutations of OCTN2, an organic cation/carnitine transporter, lead to deficient cellular carnitine uptake in primary carnitine deficiencyN L Tang, V Ganapathy, X Wu, et al.Journal of Inherited Metabolic Disease|February 22, 2012
Clinical variability of isovaleric acidemia in a genetically homogeneous populationM Dercksen, M Duran, L Ijlst, et al.The Journal of Pediatrics|October 1, 1994
A new type of peroxisomal disorder with variable expression in liver and fibroblastsH Mandel, M Espeel, F Roels, et al.Journal of Lipid Research|October 4, 2006
Metabolism of phytol to phytanic acid in the mouse, and the role of PPARalpha in its regulationJ Gloerich, D M van den Brink, J P N Ruiter, et al.The Journal of Biological Chemistry|June 5, 2010
Contributions of carnitine acetyltransferases to intracellular acetyl unit transport in Candida albicansKarin Strijbis, Carlo W van Roermund, Janny van den Burg, et al.Clinical Lung Cancer|August 3, 2012
State of the art radiation therapy for lung cancer 2012: a glimpse of the futureDirk De Ruysscher, José Belderbos, Bart Reymen, et al.Tijdschrift Voor Kindergeneeskunde|October 1, 1989
[X-linked adrenoleukodystrophy and other peroxisomal diseases caused by a failing peroxisomal beta-oxidation system: clinical expression, diagnosis and treatment]R J Wanders, P G Barth, R B Schutgens, et al.Human Genetics|June 21, 2001
Molecular and functional characterisation of mild MCAD deficiencyJ Zschocke, A Schulze, M Lindner, et al.Pediatrics|February 4, 2003
Mevalonate kinase deficiency: enlarging the clinical and biochemical spectrumViola Prietsch, Ertan Mayatepek, Hermann Krastel, et al.Acta Paediatrica (Oslo, Norway : 1992)|August 7, 2002
Long-chain 3-hydroxyacylCoA dehydrogenase deficiency: a new case presenting with liver dysfunction, cholestasis and fibrosisM H Odievre, C Sevin, J Laurent, et al.Pageof 133