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X‐linked adrenoleukodystrophy: Identification of the primary defect at the level of a deficient peroxisomal very long chain fatty acyl‐CoA synthetase using a newly developed method for the isolation of peroxisomes from skin fibroblasts
Author(s) -
Wanders R. J. A.,
Roermund C. W. T.,
Wijland M. J. A.,
Schutgens R. B. H.,
Schram A. W.,
Tager J. M.,
Bosch H.,
Schalkwijk C.
Publication year - 1988
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/bf01804228
Subject(s) - adrenoleukodystrophy , peroxisome , peroxisomal disorder , university hospital , medicine , pediatrics , receptor
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