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Fabry Cardiomyopathy: Current Practice and Future Directions
Fabry disease (FD) is an X-linked lysosomal storage disorder caused by mutations in the galactosidase A (GLA) gene that result in deficient galactosidase A enzyme and subsequent accumulation of glycosphingolipids throughout the body. The result is a multi-system disorder characterized by cutaneous,...
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| Publicat a: | Cells |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
MDPI
2021
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8233708/ https://ncbi.nlm.nih.gov/pubmed/34204530 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/cells10061532 |
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