The molecular heterogeneity of purified human liver lysosomal α-Glucosidase (acid α-Glucosidase)
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Biochemistry,Biophysics
Reference26 articles.
1. α-Glucosidase deficiency in generalized glycogen-storage disease (Pompe's disease)
2. ACID MALTASE DEFICIENCY IN ADULTS: STUDIES IN FOUR CASES OF A SYNDROME WHICH MAY MIMIC MUSCULAR DYSTROPHY OR OTHER MYOPATHIES
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4. Inhibition of some hepatic lysosomal glycosidases by ethanolamines and phenyl 6-deoxy-6-(morpholin-4-yl)-β-d-glucopyranoside;Carbohydrate Research;1999-04
5. New deoxynojirimycin derivatives as potent inhibitors of intestinal α-glucohydrolases;Bioorganic & Medicinal Chemistry Letters;1997-02
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