Application of a GM1 ganglioside β-galactosidase microassay method to diagnosis of GM1 gangliosidosis
✍ Scribed by Mutoh Tatsuro; Kiuchi Kazutoshi; Sobue Itsuro; Naoi Makoto
- Book ID
- 115824730
- Publisher
- Elsevier Science
- Year
- 1984
- Tongue
- English
- Weight
- 526 KB
- Volume
- 140
- Category
- Article
- ISSN
- 0009-8981
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
A case of GMl-gangliosidosis with high activity of hepatic neutral fi-galactosidase is reported. Gl~ii-fi-galactosidase was deficient. Ganglioside G5I 1 was accumulated in the liver of this patient. Clinically this Japanese girl started convulsive seizures at 5 months of age, had hepatomegaly, and m
Prenatal diagnoses were established in 3 pregnancies at risk for GM1-gangliosidosis at 9, 10, and 12 days after amniocentesis. Beta-galactosidase activities in cultured amniotic fluid cells were determined by microchemical assays in cell homogenates and in isolated groups of 10--30 freeze-dried cell