Carnitine-acylcarnitine carrier deficiency: identification of the molecular defect in a patient

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Title:	Carnitine-acylcarnitine carrier deficiency: identification of the molecular defect in a patient
Author(s):	Huizing, M. ; Wendel, U.A.H.; Ruitenbeek, W. ; Iacobazzi, V.; Ijlst, L.; Veenhuizen, P.; Savelkoul, P.J.M. ; Heuvel, L.P.W.J. van den ; Smeitink, J.A.M. ; Wanders, R.J.; Trijbels, J.M.F. ; Palmieri, F.
Publication year:	1998
Source:	Journal of Inherited Metabolic Disease, vol. 21, (1998), pp. 262-267
Number of Pages:	6 p.
ISSN:	0141-8955
DOI:	https://doi.org/10.1023/A:1005324323401
Publication type:	Article / Letter to editor
Please use this identifier to cite or link to this item : https://hdl.handle.net/2066/188750
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Subject:	Mitochondrial transport systems in mitochondriopathies. Mitochondriële transportsystemen in mitochondriopathieën.
Organization:	Paediatrics - OUD tm 2017 Cell Physiology
Journal title:	Journal of Inherited Metabolic Disease
Volume:	vol. 21
Page start:	p. 262
Page end:	p. 267