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Fabry disease – current data and therapeutic approaches
Fabry disease represents an X-linked inherited disorder resulting in the accumulation of globotriaosylceramide (Gb3). This review explains the clinical manifestations and the possible therapies for this condition. Fabry disease is considered the second most frequent lysosomal storage disease. More t...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Academy of Medical Sciences, Romanian Academy Publishing House, Bucharest
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8597377/ https://www.ncbi.nlm.nih.gov/pubmed/34609404 http://dx.doi.org/10.47162/RJME.62.1.01 |