Files in this item

Thumbnail
Name: 50339.pdf
Format: PDF
Description: publisher's version
Embargo: until further notice
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: The 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://repository.ubn.ru.nl/handle/2066/50339   http://repository.ubn.ru.nl/handle/2066/50339

Display more details
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: The American journal of medicine
Volume: vol. 119
Issue: iss. 2
Page start: p. 176
Page end: p. 179

Browse

Statistics