{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,10,22]],"date-time":"2023-10-22T10:52:22Z","timestamp":1697971942453},"reference-count":25,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[1985,2,11]],"date-time":"1985-02-11T00:00:00Z","timestamp":476928000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J of Inher Metab Disea"],"published-print":{"date-parts":[[1986,6]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>We measured the activity of dihydroxyacetone phosphate acyltransferase (DHAP\u2010AT) in fibroblasts of controls and patients with classical Refsum's disease (RD), infantile Refsum's disease (IRD) and Zellweger's syndrome (ZS). We confirmed that DHAP\u2010AT activity is severely reduced in ZS fibroblasts and amniocytes. We also demonstrated a partial deficiency of DHAP\u2010AT activity in RD and IRD fibroblast cultures. These diseases are probably distinct but related entities in which peroxisomal biogenesis is affected to varying degrees.<\/jats:p>","DOI":"10.1007\/bf01799453","type":"journal-article","created":{"date-parts":[[2005,6,21]],"date-time":"2005-06-21T16:51:43Z","timestamp":1119372703000},"page":"163-168","source":"Crossref","is-referenced-by-count":14,"title":["Partial deficiency of dihydroxyacetone phosphate acyltransferase activity in both classical and infantile Refsum's diseases"],"prefix":"10.1002","volume":"9","author":[{"given":"J. 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