Deficiency of acyl-CoA: dihydroxyacetone phosphate acyltransferase in thrombocytes of Zellweger patients: a simple postnatal diagnostic test
- 30 September 1985
- journal article
- research article
- Published by Elsevier in Clinica Chimica Acta; International Journal of Clinical Chemistry
- Vol. 151 (3) , 217-221
- https://doi.org/10.1016/0009-8981(85)90083-x
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
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- The cerebrohepatorenal syndrome of Zellweger, morphologic and metabolic aspectsAmerican Journal of Medical Genetics, 1983
- Severe plasmalogen deficiency in tissues of infants without peroxisomes (Zellweger syndrome)Nature, 1983
- Subcellular localization of acyl coenzyme A: dihydroxyacetone phosphate acyltransferase in rat liver peroxisomes (microbodies).Journal of Biological Chemistry, 1979
- Peroxisomal and Mitochondrial Defects in the Cerebro-Hepato-Renal SyndromeScience, 1973