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IJlst, L
Jakobs, C
Duran, M
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Wanders, RJA
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Muntau, AC
Duran, M
Dorland, L
IJlst, L
Wanders, RJA
Roscher, AA
Citation: W. Roschinger et al., Carnitine-acylcarnitine translocase deficiency: metabolic consequences of an impaired mitochondrial carnitine cycle, CLIN CHIM A, 298(1-2), 2000, pp. 55-68
Authors:
Bennett, MJ
Spotswood, SD
Ross, KF
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Koonce, R
Boriack, RL
IJlst, L
Wanders, RJA
Citation: Mj. Bennett et al., Fatal hepatic short-chain L-3-hydroxyacyl-coenzyme A dehydrogenase deficiency: Clinical, biochemical, and pathological studies on three subjects withthis recently identified disorder of mitochondrial beta-oxidation, PEDIATR D P, 2(4), 1999, pp. 337-345
Authors:
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Olpin, S
Kvittingen, EA
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Lindhout, D
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Wanders, RJA
IJlst, L
Schroeder, LD
Bolund, L
Gregersen, N
Citation: Bs. Andresen et al., DNA-based prenatal diagnosis for very-long-chain acyl-CoA dehydrogenase deficiency, J INH MET D, 22(3), 1999, pp. 281-285
Authors:
IJlst, L
Oostheim, W
van Werkhoven, M
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Wanders, RJA
Citation: L. Ijlst et al., Molecular basis of Sjogren-Larsson syndrome: Frequency of the 1297-1298 del GA and 943C -> T mutation in 29 patients, J INH MET D, 22(3), 1999, pp. 319-321
Authors:
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Mulders, J
IJlst, L
Denis, S
Dacremont, G
Waterham, HR
Wanders, RJA
Citation: S. Ferdinandusse et al., Molecular cloning and expression of human carnitine octanoyltransferase: Evidence for its role in the peroxisomal beta-oxidation of branched-chain fatty acids, BIOC BIOP R, 263(1), 1999, pp. 213-218