NDLI: 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

Content Provider	Scilit
Author	Wanders, R. J. A. van Roermund, C. W. T. van Wijland, M. J. A. Schutgens, R. B. H. Schram, A. W. Tager, J. M. Bosch, H. Van Den Schalkwijk, C.
Copyright Year	1988
Description	Journal: Journal of Inherited Metabolic Disease
Ending Page	177
Starting Page	173
ISSN	00221295
e-ISSN	15732665
DOI	10.1007/bf01804228
Journal	Journal of Inherited Metabolic Disease
Issue Number	S2
Volume Number	11
Language	English
Publisher	Wiley-Blackwell
Publisher Date	1988-06-01
Access Restriction	Open
Subject Keyword	Journal: Journal of Inherited Metabolic Disease Analytical Chemistry
Content Type	Text
Resource Type	Article
Subject	Physiology

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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