Yüklüyor......
Hepatocyte GP73 expression in Wilson disease
BACKGROUND/AIMS: Wilson disease (WD) is a disorder of copper transport caused by mutations within the ATP7B gene. WD is phenotypically variable and can present with predominantly hepatic or neurologic manifestations. The mechanisms responsible for this variability are unknown. GP73, a Golgi membrane...
Kaydedildi:
| Asıl Yazarlar: | , , , , , |
|---|---|
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2009
|
| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2750828/ https://ncbi.nlm.nih.gov/pubmed/19596473 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jhep.2009.05.029 |
| Etiketler: |
Etiketle
Etiket eklenmemiş, İlk siz ekleyin!
|