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Alpha-1 Antitrypsin Deficiency-Mediated Liver Toxicity: Why Do Some Patients Do Poorly? What Do We Know So Far?
Alpha-1 antitrypsin deficiency (AATD) is a rare genetic disease caused by mutations in the SERPINA1 gene and is associated with a decreased level of circulating alpha-1 antitrypsin (AAT). Among all the known mutations in the SERPINA1 gene, homozygous for the Z allele is well-known to result in both...
Tallennettuna:
| Julkaisussa: | Chronic Obstr Pulm Dis |
|---|---|
| Päätekijä: | |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
COPD Foundation Inc
2020
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7857713/ https://ncbi.nlm.nih.gov/pubmed/32558486 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15326/jcopdf.7.3.2019.0148 |
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