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Clinical considerations in individuals with α(1)-antitrypsin PI*SZ genotype
α(1)-Antitrypsin deficiency (AATD), characterised by reduced levels or functionality of α(1)-antitrypsin (AAT), is a significantly underdiagnosed genetic condition that predisposes individuals to lung and liver disease. Most of the available data on AATD are based on the most common, severe deficien...
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| Publicat a: | Eur Respir J |
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| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
European Respiratory Society
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7301289/ https://ncbi.nlm.nih.gov/pubmed/32165400 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1183/13993003.02410-2019 |
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