The apparent activity in vivo of the lysosomal pathway of glycogen catabolism in cultured human skin fibroblasts from patients with type III glycogen storage disease.
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference36 articles.
1. α-Glucosidase deficiency in generalized glycogen-storage disease (Pompe's disease)
2. ADULT MYOPATHY FROM GLYCOGEN STORAGE DISEASE DUE TO ACID MALTASE DEFICIENCY
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