Abstract
Anderson-Fabry disease (AFD) is a rare genetic lysosomal storage disorder caused by deficient activity of the enzyme α-galactosidase A, leading to progressive intracellular accumulation of neutral glycosphingolipids in different organs, including the heart.
| Lingua originale | Inglese |
|---|---|
| pagine (da-a) | N/A-e009104 |
| Rivista | Circulation: Cardiovascular Imaging |
| Volume | 12 |
| DOI | |
| Stato di pubblicazione | Pubblicato - 2019 |
Keywords
- Fabry disease
- galactosidases
- hypertrophy
- morbidity
- mortality
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