Structure of the “keratosulfate-like” material in liver from a patient with GM1-gangliosidosis (β-D-galactosidase deficiency)
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference18 articles.
1. The Metabolic Basis of Inherited Diseases;O'Brien,1972
2. Chemical Pathology of GM1-Gangliosidosis (Generalized Gangliosidosis)
3. GM1-gangliosidosis without chondrodystrophy or visceromegaly: -galactosidase deficiency with gangliosidosis and the excessive excretion of a keratan sulfate
4. Die Konstitution der Ganglio‐N‐tetraose und des Gangliosids G I
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