Rhabdomyolysis caused by an inherited metabolic disease: very long-chain acyl-CoA dehydrogenase deficiency.

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Title:	Rhabdomyolysis caused by an inherited metabolic disease: very long-chain acyl-CoA dehydrogenase deficiency.
Author(s):	Voermans, N.C. (298207303) Engelen, B.G.M. van (142921203) Kluijtmans, L.A.J. (168872579) Stikkelbroeck, N.M. Hermus, A.R.M.M. (07172429X)
Publication year:	2006
Document type:	Article / Letter to editor
Journal:	The American journal of medicine
ISSN:	0002-9343
Volume:	vol. 119
Issue:	iss. 2
Start page:	p. 176
End page:	p. 179
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
Appears in Collections:	Academic bibliography

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