The Glycosphingolipidoses from Disease to Basic Principles of Metabolism
Author:
Publisher
Walter de Gruyter GmbH
Subject
Clinical Biochemistry,Molecular Biology,Biochemistry
Link
https://www.degruyter.com/document/doi/10.1515/BC.1999.096/pdf
Reference24 articles.
1. AB variant of infantile GM2 gangliosidosis: deficiency of a factor necessary for stimulation of hexosaminidase A-catalyzed degradation of ganglioside GM2 and glycolipid GA2.
2. Purification and Characterization of an Activator Protein for the Degradation of Glycolipids GM2and GA2by Hexosaminidase A
3. Partial Enzyme Deficiencies: Residual Activities and the Development of Neurological Disorders
4. Sphingolipid Activator Proteins Are Required for Epidermal Permeability Barrier Formation
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