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Human dihydroxyacetonephosphate acyltransferase deficiency: a new peroxisomal disorder

R J Wanders¹, H Schumacher, J Heikoop

¹Dept of Pediatrics and Clinical Biochemistry, University of Amsterdam, The Netherlands.

Journal of Inherited Metabolic Disease

|January 1, 1992

Abstract

No abstract available in PubMed .

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