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Effects of agalsidase-β administration on vascular function and blood pressure in familial Anderson–Fabry disease
Fabry is an X-linked disorder of glycosphingolipid metabolism that is caused by variants of the GLA gene that codes for α-galactosidase A, leading to lysosomal accumulation of globotriaosylceramide in many cell types. As a result, affected patients manifest with an increased risk of developing ische...
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| Publicado no: | Eur J Hum Genet |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer International Publishing
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7868353/ https://ncbi.nlm.nih.gov/pubmed/32948848 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41431-020-00721-9 |
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