Human alkyldihydroxyacetonephosphate synthase deficiency: A new peroxisomal disorder
- 1 May 1994
- journal article
- case report
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 17 (3) , 315-318
- https://doi.org/10.1007/bf00711817
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Postnatal diagnosis of peroxisomal disorders: A biochemical approachBiochimie, 1993
- THE STRUCTURE AND BIOSYNTHESIS OF GLYCOSYL PHOSPHATIDYLINOSITOL PROTEIN ANCHORSAnnual Review of Biochemistry, 1993
- BIOCHEMISTRY OF PEROXISOMESAnnual Review of Biochemistry, 1992
- Human dihydroxyacetonephosphate acyltransferase deficiency: A new peroxisomal disorderJournal of Inherited Metabolic Disease, 1992
- Class F Thy-1-negative murine lymphoma cells are deficient in ether lipid biosynthesis.Journal of Biological Chemistry, 1990
- Peroxisomal disorders in neurologyJournal of the Neurological Sciences, 1988
- Heterogeneity of Chondrodysplasia punctataHuman Genetics, 1971