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. 1988:11 Suppl 2:173-7.
doi: 10.1007/BF01804228.

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

R J Wanders  1 , C W van Roermund, M J van Wijland, R B Schutgens, A W Schram, J M Tager, H van den Bosch, C Schalkwijk
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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

R J Wanders et al. J Inherit Metab Dis. 1988.
No abstract available

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References

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    1. Ann Neurol. 1984 Dec;16(6):628-41 - PubMed
    1. J Clin Invest. 1987 Dec;80(6):1778-83 - PubMed

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