Long-term effectiveness and safety of agalsidase alfa in patients with Fabry disease treated for at least 19 years: The Fabry Outcome Survey
Fields of Study & Subjects
Lysosomal Storage Disorders Research
Glycogen Storage Diseases and Myoclonus
Metabolism and Genetic Disorders
Publication details
- Journal / source
- Molecular Genetics and Metabolism
- Volume
- 147
- Issue
- 2
- Pages
- 109477–109477
- Publication date
- 1 February 2026
- Language
- EN