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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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Kaydedildi:
Detaylı Bibliyografya
Yazar: Pastores, Gregory M
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Dove Medical Press 2007
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2721310/
https://ncbi.nlm.nih.gov/pubmed/19707338
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