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Kidney Transplant in Fabry Disease: A Revision of the Literature
Fabry disease is classified as a rare X-linked disease caused by a complete or partial defect of enzyme alpha-galactosidase, due to GLA gene mutations. This disorder leads to intracellular globotriaosylceramide (Gb3) deposition associated with increased Gb3 plasma levels. Most of the symptoms of the...
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| Publicado no: | Medicina (Kaunas) |
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| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7353860/ https://ncbi.nlm.nih.gov/pubmed/32532136 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/medicina56060284 |
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