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Anderson–Fabry Disease: From Endothelial Dysfunction to Emerging Therapies
The Anderson–Fabry disease is a rare, X-linked, multisystemic, progressive lysosomal storage disease caused by α-galactosidase A total or partial deficiency. The resulting syndrome is mainly characterized by early-onset autonomic neuropathy and life-threatening multiorgan involvement, including rena...
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| Publicado no: | Adv Pharmacol Pharm Sci |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Hindawi
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8137293/ https://ncbi.nlm.nih.gov/pubmed/34095851 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2021/5548445 |
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