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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...
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| Главные авторы: | , , , , , |
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| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
2009
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| Предметы: | |
| Online-ссылка: | 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 |
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