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Genomic abnormalities of the murine model of Fabry disease after disease-related perturbation, a systems biology approach
Fabry disease is a disorder of α-d-galactosyl-containing glycolipids resulting from a deficiency of α-galactosidase A. Patients have a poorly understood vascular dysregulation. We hypothesized that disease-related perturbation by using enzyme replacement therapy in the murine model of Fabry disease...
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| Main Authors: | , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
National Academy of Sciences
2007
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1859990/ https://ncbi.nlm.nih.gov/pubmed/17470787 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0701991104 |
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