A case review of a man with late onset Pompe disease who has switched enzyme replacement therapies: Clinical and physiotherapy outcomes
Fields of Study & Subjects
Lysosomal Storage Disorders Research
Glycogen Storage Diseases and Myoclonus
Biomedical Research and Pathophysiology
Publication details
- Journal / source
- Molecular Genetics and Metabolism
- Volume
- 147
- Issue
- 2
- Pages
- 109486–109486
- Publication date
- 1 February 2026
- Language
- EN