Update on genetic and molecular investigations of diseases with general impairment of peroxisomal functions
- 31 December 1993
- Vol. 75 (3-4) , 303-308
- https://doi.org/10.1016/0300-9084(93)90090-f
Abstract
No abstract availableKeywords
This publication has 30 references indexed in Scilit:
- Peroxisomal disordersClinical Biochemistry, 1991
- Peroxisome biogenesis revisitedBiochimica et Biophysica Acta (BBA) - Gene Structure and Expression, 1989
- The Cerebro‐Hepato‐Renal (Zellweger) Syndrome And Other Peroxisomal DisordersDevelopmental Medicine and Child Neurology, 1987
- β-oxidation of very-long-chain fatty acids and their coenzyme A derivatives by human skin fibroblastsArchives of Biochemistry and Biophysics, 1987
- Neonatal adrenoleukodystrophy: New cases, biochemical studies, and differentiation from Zellweger and related peroxisomal polydystrophy syndromesAmerican Journal of Medical Genetics, 1986
- Biogenesis of PeroxisomesAnnual Review of Cell Biology, 1985
- The cerebrohepatorenal syndrome of Zellweger, morphologic and metabolic aspectsAmerican Journal of Medical Genetics, 1983
- Infantile phytanic acid storage disease, a possible variant of Refsum's disease: Three cases, including ultrastructural studies of the liverJournal of Inherited Metabolic Disease, 1982
- AdrenoleukodystrophyActa Neuropathologica, 1978
- Intracellular localization of catalase and some oxidases in rat liverBiochimica et Biophysica Acta, 1960