1               The physiological relevance of acid maltase (acid alpha-glucosidase, an enzyme that deg

2  acid alpha -glucosidase (GAA) (also called "acid maltase"), causes death in early childhood related

3                        In late (adult)-onset acid maltase deficiency (glycogen storage disease type I

4 l muscular atrophy (SMA), and Pompe disease (acid maltase deficiency [AMD]), are candidates for unive

5 eas they form long lists for others, such as acid maltase deficiency and myophosphorylase deficiency;

6              The diagnosis of Pompe disease (acid maltase deficiency, glycogen storage disease type I

7 nherited disorder caused by mutations in the acid maltase (GAA) gene.

8 tivities of debranching enzyme and lysosomal acid maltase, two major hepatic alpha-glucosidases, were

9 sosomal glycogen storage disease with normal acid maltase" which was originally described by Danon et