GM1-ganglioside β-galactosidase in leukocytes and cultured fibroblasts
Author:
Publisher
Elsevier BV
Subject
Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine
Reference24 articles.
1. Macular cherry-red spot, corneal clouding, and -galactosidase deficiency. Clinical, biochemical, and electron microscopic study of a new autosomal recessive storage disease
2. ANGIOKERATOMA CORPORIS DIFFUSUM AND LYSOSOMAL ENZYME DEFICIENCY
3. A New Type of Mucolipidosis with β-Galactosidase Deficiency and Glycopeptiduria
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1. Leukocyte Lysosomal Enzymes in Alzheimer's Disease and Down's Syndrome;The Journals of Gerontology Series A: Biological Sciences and Medical Sciences;2002-01-01
2. Effect of collection, transport, processing and storage of blood specimens on the activity of lysosomal enzymes in plasma and leukocytes;Brazilian Journal of Medical and Biological Research;2000-09
3. Characterization of β-galactosidase in leukocytes and fibroblasts of GM1 gangliosidosis heterozygotes compared to normal subjects;Clinical Biochemistry;2000-03
4. A case of GM1gangliosidosis type I;Ophthalmic Paediatrics and Genetics;1989-01
5. Disorders of Lipid Metabolism;Genetic Disorders and the Fetus;1986
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