https://scholars.lib.ntu.edu.tw/entities/publication/524038bb-f0f4-479d-a274-92edb838f902
Enzyme Replacement Therapy with Recombinant Human Acid Alpha Glucosidase (Rhgaa) in Infantile Onset...
Introduction: Glycogen Storage disease type 2 (GSD II), also known as Pompe disease is caused by a deficiency of the lysosomal enzyme acid alpha glucosidase...
enzyme replacement therapy