Pre‐ and postnatal diagnosis of the cerebrohepato‐renal (Zellweger) syndrome via a simple method directly demonstrating the presence of absence of peroxisomes in cultured skin fibroblasts, amniocytes or chorionic villi fibroblasts
- 1 June 1986
- journal article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 9 (S2) , 317-320
- https://doi.org/10.1007/bf01799740
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Deficiency of acyl-CoA: dihydroxyacetone phosphate acyltransferase in thrombocytes of Zellweger patients: a simple postnatal diagnostic testClinica Chimica Acta; International Journal of Clinical Chemistry, 1985
- PRENATAL DETECTION OF ZELLWEGER SYNDROMEThe Lancet, 1984
- Activity of peroxisomal enzymes and intracellular distribution of catalase in Zellweger syndromeBiochemical and Biophysical Research Communications, 1984
- Deficiency of acyl-CoA: Dihydroxyacetone phosphate acyltransferase in patients with Zellweger (cerebro-hepato-renal) syndromeBiochemical and Biophysical Research Communications, 1984
- The cerebrohepatorenal syndrome of Zellweger, morphologic and metabolic aspectsAmerican Journal of Medical Genetics, 1983
- Peroxisomal and Mitochondrial Defects in the Cerebro-Hepato-Renal SyndromeScience, 1973