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• W2013375669 abstract "Journal of Inherited Metabolic DiseaseVolume 10, Issue S2 p. 214-216 Short Communication A genetic disorder due to the deficiency of the peroxisomal β-oxidation enzyme 3-oxoacyl-CoA thiolase A. W. Schram, A. W. Schram Laboratory of Biochemistry, University of Amsterdam, PO Box 20151, 1000 HD The NetherlandsSearch for more papers by this authorS. Goldfischer, S. Goldfischer Department of Pathology, Albert Einstein College of Medicine, Bronx, New York, 10461 USASearch for more papers by this authorR. J. A. Wanders, R. J. A. Wanders Department of Paediatrics, Academic Medical Centre of the University of Amsterdam, Amsterdam, 1105 AZ The NetherlandsSearch for more papers by this authorE. M. Brouwer-Kelder, E. M. Brouwer-Kelder Laboratory of Biochemistry, University of Amsterdam, PO Box 20151, 1000 HD The NetherlandsSearch for more papers by this authorC. W. T. van Roermund, C. W. T. van Roermund Department of Paediatrics, Academic Medical Centre of the University of Amsterdam, Amsterdam, 1105 AZ The NetherlandsSearch for more papers by this authorJ. Collins, J. Collins Department of Pathology, Albert Einstein College of Medicine, Bronx, New York, 10461 USASearch for more papers by this authorT. Hashimoto, T. Hashimoto Shinshu University School of Medicine, Asahi, Matsumoto, 390 JapanSearch for more papers by this authorH. S. A. Heymans, H. S. A. Heymans Department of Paediatrics, Academic Medical Centre of the University of Amsterdam, Amsterdam, 1105 AZ The NetherlandsSearch for more papers by this authorR. B. H. Schutgens, R. B. H. Schutgens Department of Paediatrics, Academic Medical Centre of the University of Amsterdam, Amsterdam, 1105 AZ The NetherlandsSearch for more papers by this authorH. van den Bosch, H. van den Bosch Laboratory of Biochemistry, University of Utrecht, Padualaan 8, Utrecht, 3584 CH The NetherlandsSearch for more papers by this authorJ. M. Tager, J. M. Tager Laboratory of Biochemistry, University of Amsterdam, PO Box 20151, 1000 HD The NetherlandsSearch for more papers by this author A. W. Schram, A. W. Schram Laboratory of Biochemistry, University of Amsterdam, PO Box 20151, 1000 HD The NetherlandsSearch for more papers by this authorS. Goldfischer, S. Goldfischer Department of Pathology, Albert Einstein College of Medicine, Bronx, New York, 10461 USASearch for more papers by this authorR. J. A. Wanders, R. J. A. Wanders Department of Paediatrics, Academic Medical Centre of the University of Amsterdam, Amsterdam, 1105 AZ The NetherlandsSearch for more papers by this authorE. M. Brouwer-Kelder, E. M. Brouwer-Kelder Laboratory of Biochemistry, University of Amsterdam, PO Box 20151, 1000 HD The NetherlandsSearch for more papers by this authorC. W. T. van Roermund, C. W. T. van Roermund Department of Paediatrics, Academic Medical Centre of the University of Amsterdam, Amsterdam, 1105 AZ The NetherlandsSearch for more papers by this authorJ. Collins, J. Collins Department of Pathology, Albert Einstein College of Medicine, Bronx, New York, 10461 USASearch for more papers by this authorT. Hashimoto, T. Hashimoto Shinshu University School of Medicine, Asahi, Matsumoto, 390 JapanSearch for more papers by this authorH. S. A. Heymans, H. S. A. Heymans Department of Paediatrics, Academic Medical Centre of the University of Amsterdam, Amsterdam, 1105 AZ The NetherlandsSearch for more papers by this authorR. B. H. Schutgens, R. B. H. Schutgens Department of Paediatrics, Academic Medical Centre of the University of Amsterdam, Amsterdam, 1105 AZ The NetherlandsSearch for more papers by this authorH. van den Bosch, H. van den Bosch Laboratory of Biochemistry, University of Utrecht, Padualaan 8, Utrecht, 3584 CH The NetherlandsSearch for more papers by this authorJ. M. Tager, J. M. Tager Laboratory of Biochemistry, University of Amsterdam, PO Box 20151, 1000 HD The NetherlandsSearch for more papers by this author First published: 01 June 1987 https://doi.org/10.1007/BF01811408Citations: 2AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat No abstract is available for this article.Citing Literature Volume10, IssueS2June 1987Pages 214-216 RelatedInformation" @default.
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• W2013375669 title "A genetic disorder due to the deficiency of the peroxisomal β-oxidation enzyme 3-oxoacyl-CoA thiolase" @default.
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