Yüklüyor......
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...
Kaydedildi:
| Asıl Yazarlar: | , |
|---|---|
| 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 |
| Etiketler: |
Etiketle
Etiket eklenmemiş, İlk siz ekleyin!
|