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Velaglucerase alfa in the treatment of Gaucher disease type 1

Gaucher disease is an autosomal recessively inherited lysosomal storage disease that results from the defective activity of the enzyme acid β-glucosidase (glucocerebrosidase). Velaglucerase alfa was recently developed and approved as an alternative form to imiglucerase enzyme therapy. Despite differ...

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Detaylı Bibliyografya
Asıl Yazarlar: Burrow, Thomas A, Grabowski, Gregory A
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2011
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3172711/
https://ncbi.nlm.nih.gov/pubmed/21927713
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