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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...
Wedi'i Gadw mewn:
| Prif Awduron: | , , , , , |
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| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
2009
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| Pynciau: | |
| Mynediad Ar-lein: | 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 |
| Tagiau: |
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