Synthesis of and its use in classification of GM2 gangliosidosis genotypes
- 1 November 1984
- journal article
- research article
- Published by Elsevier in Clinica Chimica Acta; International Journal of Clinical Chemistry
- Vol. 143 (2), 73-89
- https://doi.org/10.1016/0009-8981(84)90215-8
Abstract
No abstract availableKeywords
This publication has 24 references indexed in Scilit:
- Juvenile progressive dystonia: A new phenotype of GM2 GangliosidosisAnnals of Neurology, 1984
- Tay-Sachs disease: one-step assay of β-N-acetylhexosaminidase in serum with a sulphated chromogenic substrateClinica Chimica Acta; International Journal of Clinical Chemistry, 1983
- Deficiency of the Hexosaminidase A Activator Protein in a Case of GM2 Gangliosidosis; Variant ABPediatric Research, 1982
- Human hexosaminidase isozymes: Chromatographic separation as an aid to heterozygote identificationClinica Chimica Acta; International Journal of Clinical Chemistry, 1977
- Chemical characterization and subunit structure of human N-acetylhexosaminidases A and BBiochemistry, 1976
- N-acetylgalactosamine 4,6-bissulfate in rat urine I. Isolation, identification and chemical synthesisBiochimica et Biophysica Acta (BBA) - General Subjects, 1976
- The demonstration of multiple heat stable forms of N-acetyl-β-glucosaminidase in normal human serumBiochimica et Biophysica Acta (BBA) - Protein Structure, 1972
- Tay-Sachs Disease: Generalized Absence of a Beta-D- N -Acetylhexosaminidase ComponentScience, 1969
- Fractionation of the products of the direct sulphation of monosaccharides on anion-exchange resinBiochemical Journal, 1962
- Studies on glucosaminidase. 4. The fluorimetric assay of N-acetyl-β-glucosaminidaseBiochemical Journal, 1961