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Establishment and Characterization of Fabry Disease Endothelial Cells with an Extended Lifespan
Fabry disease is an inborn error of glycosphingolipid catabolism resulting from a deficiency of lysosomal enzyme α-galactosidase A. The major clinical manifestations of the disease, such as stroke, cardiac dysfunction, and renal impairment, are thought to be caused by vasculopathy due to progressive...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2007
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2063578/ https://ncbi.nlm.nih.gov/pubmed/17644384 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2007.06.003 |
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