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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
This item appears in the following Collection(s)
Faculty of Medical Sciences
[73895]
Academic publications
[187655]
Academic output Radboud University
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