Subcellular distribution of acid and neutral α-glucosidases in normal, acid maltose deficient, and myophosphorylase deficient human skeletal muscle
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Biochemistry,Biophysics
Reference22 articles.
1. α-Glucosidase deficiency in generalized glycogen-storage disease (Pompe's disease)
2. Lysosomal α-glucosidase. I. Purification and properties of the rat liver enzyme
3. Comparative Study of Acid Maltase Deficiency
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5. The electrophoretic pattern and activities of acid and neutral maltase of cultivated fibroblasts and amniotic fluid cells from controls and patients with the variant of glycogen storage disease Type II (Pompe's disease)
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