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Peroxisomal fatty acid β‐oxidation in human skin fibroblasts: X‐linked adrenoleukodystrophy, a peroxisomal very long chain fatty acyl‐CoA synthetase deficiency?
Author(s) -
Wanders R. J. A.,
Van Roermund C. W. T.,
Van Wijland M. J. A.,
Heikoop J.,
Van den Put A.,
Bentlage P.,
Meijboom E.,
Tager J. M.,
Schram A. W.,
Van den Bosch H.,
Schutgens R. B. H.
Publication year - 1987
Publication title -
journal of inherited metabolic disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.462
H-Index - 102
eISSN - 1573-2665
pISSN - 0141-8955
DOI - 10.1007/bf01811410
Subject(s) - adrenoleukodystrophy , peroxisome , peroxisomal disorder , university hospital , medicine , pediatrics , receptor
R. J. A. WANDERS l*, C. W. T. VAN ROERMtJND 1, M. J. A. VAN WIJLAND 1, J. HEIKOOP 1, A. VAN DEN PUT 1, P. BENTLAGE 1, E. MEIJBOOM 1, J. M. TAGER 2, A. W. SCHRAM 2, H. VAN DEN BOSCH 3 and R. B. H. SCHUTGENS 1 aDepartment of Pediatrics, University of Amsterdam, Meibergdreef 9, 1105 A Z Amsterdam, The Netherlands; 2Laboratory of Biochemistry, University of Amsterdam, Meibergdreef 15, 1105 A Z Amsterdam, The Netherlands; ~Laboratory of Biochemistry, State University Utrecht, Padualaan 8, 3584 CH Utrecht, The Netherlands