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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

✍ Scribed by R. J. A. Wanders; C. W. T. van Roermund; M. J. A. van Wijland; R. B. H. Schutgens; A. W. Schram; J. M. Tager; H. van den Bosch; C. Schalkwijk


Publisher
Springer
Year
1988
Tongue
English
Weight
408 KB
Volume
11
Category
Article
ISSN
0141-8955

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