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Fabry disease during the COVID-19 pandemic. Why and how treatment should be continued
Fabry disease is an X-linked disease due to a deficiency of the lysosomal enzyme alpha-galactosidase A. Clinical symptoms in classically affected males include acroparesthesia, anhydrosis and angiokeratoma, which may present during childhood followed by cardiac, cerebral and renal complications. Eve...
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| Yayımlandı: | Mol Genet Metab |
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| Yazar: | |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Elsevier Inc.
2020
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7274950/ https://ncbi.nlm.nih.gov/pubmed/32561366 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2020.06.002 |
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