La terapia enzimatica sostitutiva nella malattia di Fabry
Anderson-Fabry disease (FD) is a X-linked lysosomal storage disorder, which involves glycosphingolipids metabolism. Specific treatment for FD has been available in the last two decades, after the development and commercialization of recombinant human alfa-galactosidase A. Since then enzyme replaceme...
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| Principais autores: | , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
AboutScience Srl
2019-09-01
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| Serier: | Giornale di Clinica Nefrologia e Dialisi |
| Online adgang: | https://journals.aboutscience.eu/index.php/gcnd/article/view/528 |
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