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Podocyturia: why it may have added value in rare diseases
Fabry disease is an inherited lysosomal disease in which defects in the GLA gene lead to α-galactosidase-A deficiency, and accumulation of glycosphingolipids, including lyso-Gb3, a podocyte stressor. Therapy is available as enzyme replacement therapy and, for some patients, the chaperone migalastat....
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| Publicado no: | Clin Kidney J |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6407136/ https://ncbi.nlm.nih.gov/pubmed/30863545 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/ckj/sfy081 |
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