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Proteomics of specific treatment-related alterations in Fabry disease: A strategy to identify biological abnormalities
Fabry disease is inherited as an X-linked disorder secondary to deficiency of α-galactosidase A, resulting in abnormal metabolism of substances containing α-d-galactosyl moieties. As a consequence, a multisystem disorder develops, culminating in strokes, progressive renal, and cardiac dysfunction. S...
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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/PMC1797627/ https://ncbi.nlm.nih.gov/pubmed/17301227 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0611315104 |
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