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Agalsidase alfa (Replagal(™)) in the treatment of Anderson-Fabry disease
Anderson-Fabry disease (AFD) is an X-linked storage disorder caused by a deficiency of the lysosomal hydrolase a-galactosidase A (AGAL) and the resultant accumulation of its glycosphingolipid substrate (Gb3) in several tissue types. Major morbidity and reduced life expectancy among affected individu...
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| 主要作者: | |
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| 格式: | Artigo |
| 語言: | Inglês |
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Dove Medical Press
2007
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2721310/ https://ncbi.nlm.nih.gov/pubmed/19707338 |
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