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Contemporary therapeutics and new drug developments for treatment of Fabry disease: a narrative review
Fabry disease (OMIM 301500) is an X-linked (Xq22.1) lysosomal storage disorder leading to a progressive multisystem disease with high variability in both genotype and phenotype expression. The pathophysiological origin is found in an enzyme deficiency of the α-galactosidase A (enzyme commission no....
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| Publicado no: | Cardiovasc Diagn Ther |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
AME Publishing Company
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8102271/ https://ncbi.nlm.nih.gov/pubmed/33968645 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/cdt-20-743 |
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