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Fabry Cardiomyopathy: Current Treatment and Future Options
Fabry disease is a multisystem X-linked lysosomal storage disorder caused by a mutation in the alpha-galactosidase A gene. Deficiency or reduced activity of alpha-galactosidase A (GLA) is leading to progressive intracellular accumulation of globotriaosylceramide (GL3) in various organs, including th...
Gorde:
| Argitaratua izan da: | J Clin Med |
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| Egile Nagusiak: | , , , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
MDPI
2021
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8305771/ https://ncbi.nlm.nih.gov/pubmed/34300196 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/jcm10143026 |
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