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Alpha-1 antitrypsin deficiency liver disease
The clinical presentation of liver disease is highly variable in homozygous ZZ alpha-1 antitrypsin (AAT) deficiency, and not all patients with the homozygous ZZ genotype develop liver disease. Although not fully identified, there is likely a strong influence of genetic and environmental modifiers of...
Tallennettuna:
| Julkaisussa: | Transl Gastroenterol Hepatol |
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| Päätekijät: | , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
AME Publishing Company
2021
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7829072/ https://ncbi.nlm.nih.gov/pubmed/33824927 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/tgh.2020.02.23 |
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