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Prevalence of Fabry disease in male dialysis patients: Argentinean screening study
BACKGROUND: Fabry disease (FD) is an X‐linked lysosomal storage disorder caused by enzyme Alpha‐Galactosidase A (α‐Gal‐A) deficiency, due mutations in GLA gene. Progressive glycolipid accumulation leads to damage in kidney and other organs. The aim of this study was to estimate the prevalence of Fab...
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| Publicado no: | JIMD Rep |
|---|---|
| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley & Sons, Inc.
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6606982/ https://ncbi.nlm.nih.gov/pubmed/31392112 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jmd2.12035 |
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