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SARS-CoV-2 infection in alpha1-antitrypsin deficiency
Alpha1-antitrypsin deficiency arises due to mutations in alpha1-antitrypsin (AAT) gene and represents the most prominent genetic predisposition to chronic obstructive pulmonary disease and emphysema. Since AAT plays important immunomodulatory and tissue-protective roles and since it was suggested to...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Elsevier Ltd.
2021
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8116136/ https://www.ncbi.nlm.nih.gov/pubmed/34010739 http://dx.doi.org/10.1016/j.rmed.2021.106466 |