Author/Authors :
Ans T Van der Ploeg، نويسنده , , Arnold JJ Reuser، نويسنده ,
Abstract :
Summary
Pompeʹs disease, glycogen-storage disease type II, and acid maltase deficiency are alternative names for the same metabolic disorder. It is a pan-ethnic autosomal recessive trait characterised by acid α-glucosidase deficiency leading to lysosomal
