Validation and standardization of a fluorometric method for alpha glucosidase activity assay in the detection of Pompe disease

Armin Mokhtariye; Lida Hagh-Nazari; Abdol-Reza Varasteh; Hadi Mozafari; Fatemeh Keyfi

Volume 10, Issue 2 , June 2023, , Pages 22-26

  Introduction: Pompe Disease is a type of lysosomal storage disease that is caused by a deficiency of the lysosomal alpha glucosidase. Pompe disease, as a multi-systemic disorder has a broad spectrum of clinical symptoms. The objective of this research was to validate and standardize the fluorometric ...  Read More