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Novel Treatment Strategies for Liver Disease Due to a1‐Antitrypsin Deficiency
Alpha1‐antitrypsin (AT) deficiency is the most common genetic cause of liver disease in children and is also a cause of chronic hepatic fibrosis, cirrhosis, and hepatocellular carcinoma in adults. Recent advances in understanding how mutant AT molecules accumulate within hepatocytes and cause liver...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Blackwell Publishing Inc
2012
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3982223/ https://ncbi.nlm.nih.gov/pubmed/22686209 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1752-8062.2011.00363.x |
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