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Title: Rhabdomyolysis caused by an inherited metabolic disease: very long-chain acyl-CoA dehydrogenase deficiency.
Author(s): Voermans, N.C. ; Engelen, B.G.M. van ; Kluijtmans, L.A.J. ; Stikkelbroeck, N.M.; Hermus, A.R.M.M.
Publication year: 2006
Source: American Journal of Medicine, vol. 119, iss. 2, (2006), pp. 176-179
ISSN: 0002-9343
Publication type: Article / Letter to editor

Please use this identifier to cite or link to this item : http://hdl.handle.net/2066/50339   http://hdl.handle.net/2066/50339

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Subject: UMCN 3.1: Neuromuscular development and genetic disorders
UMCN 5.1: Genetic defects of metabolism
UMCN 5.2: Endocrinology and reproduction
Organization: Neurology
Paediatrics
UMCN Extern
Endocrinology
Journal title: American Journal of Medicine
Volume: vol. 119
Issue: iss. 2
Page start: p. 176
Page end: p. 179

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