Yüklüyor......
Animal models of GM2 gangliosidosis: utility and limitations
GM2 gangliosidosis, a subset of lysosomal storage disorders, is caused by a deficiency of the glycohydrolase, β-N-acetylhexosaminidase, and includes the closely related Tay–Sachs and Sandhoff diseases. The enzyme deficiency prevents the normal, stepwise degradation of ganglioside, which accumulates...
Kaydedildi:
| Yayımlandı: | Appl Clin Genet |
|---|---|
| Asıl Yazarlar: | , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Dove Medical Press
2016
|
| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4959762/ https://ncbi.nlm.nih.gov/pubmed/27499644 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/TACG.S85354 |
| Etiketler: |
Etiketle
Etiket eklenmemiş, İlk siz ekleyin!
|