Dihydroxyacetone phosphate acyltransferase deficiency in peroxisomal disorders

This publication has 9 references indexed in Scilit:

• Genetic Relation between the Zellweger Syndrome, Infantile Refsum's Disease, and Rhizomelic Chondrodysplasia Punctata
  New England Journal of Medicine, 1986
• Peroxisomal disorders: A newly recognised group of genetic diseases
  European Journal of Pediatrics, 1986
• Pseudo-Zellweger syndrome: Deficiencies in several peroxisomal oxidative activities
  The Journal of Pediatrics, 1986
• Deficiency of acyl-CoA: dihydroxyacetone phosphate acyltransferase in thrombocytes of Zellweger patients: a simple postnatal diagnostic test
  Clinica Chimica Acta; International Journal of Clinical Chemistry, 1985
• Partial deficiency of dihydroxyacetone phosphate acyltransferase activity in both classical and infantile Refsum's diseases
  Journal of Inherited Metabolic Disease, 1985
• Deficiency of Enzymes Catalyzing the Biosynthesis of Glycerol-Ether Lipids in Zellweger Syndrome
  New England Journal of Medicine, 1984
• Deficiency of plasmalogens in the cerebro-hepato-renal (Zellweger) syndrome
  European Journal of Pediatrics, 1984
• Deficiency of acyl-CoA: Dihydroxyacetone phosphate acyltransferase in patients with Zellweger (cerebro-hepato-renal) syndrome
  Biochemical and Biophysical Research Communications, 1984