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A genetic disorder due to the deficiency of the peroxisomal β-oxidation enzyme 3-oxoacyl-CoA thiolase

✍ Scribed by A. W. Schram; S. Goldfischer; R. J. A. Wanders; E. M. Brouwer-Kelder; C. W. T. van Roermund; J. Collins; T. Hashimoto; H. S. A. Heymans; R. B. H. Schutgens; H. van den Bosch; J. M. Tager

Book ID: 105317400
Publisher: Springer
Year: 1987
Tongue: English
Weight: 221 KB
Volume: 10
Category: Article
ISSN: 0141-8955
DOI: 10.1007/bf01811408

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