Activator protein-deficient metachromatic leukodystrophy: Diagnosis in leukocytes using immunologic methods
- 31 May 1984
- journal article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 104 (5), 739-742
- https://doi.org/10.1016/s0022-3476(84)80957-9
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Immunological evidence for deficiency in an activator protein for sulfatide sulfatase in a variant form of metachromatic leukodystrophy.Proceedings of the National Academy of Sciences, 1983
- A variant form of metachromatic leukodystrophy without arylsulfatase deficiencyAnnals of Neurology, 1982
- Deficiency of the Hexosaminidase A Activator Protein in a Case of GM2 Gangliosidosis; Variant ABPediatric Research, 1982
- A dot-immunobinding assay for monoclonal and other antibodiesAnalytical Biochemistry, 1982
- Crossed immunoelectrophoresis: TechniqueClinical Immunology Newsletter, 1981
- METACHROMATIC LEUKODYSTROPHY WITHOUT ARYLSULFATASE A DEFICIENCYPediatric Research, 1979
- AB variant of infantile GM2 gangliosidosis: deficiency of a factor necessary for stimulation of hexosaminidase A-catalyzed degradation of ganglioside GM2 and glycolipid GA2.Proceedings of the National Academy of Sciences, 1978