Correlation between α1-Antitrypsin Deficiency and SARS-CoV-2 Infection: Epidemiological Data and Pathogenetic Hypotheses

The most common hereditary disorder in adults, α1-antitrypsin deficiency (AATD), is characterized by reduced plasma levels or the abnormal functioning of α1-antitrypsin (AAT), a major human blood serine protease inhibitor, which is encoded by the SERine Protein INhibitor-A1 (SERPINA1) gene and produ...

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Detalles Bibliográficos
Autores principales: Vianello, Andrea, Guarnieri, Gabriella, Braccioni, Fausto, Molena, Beatrice, Lococo, Sara, Achille, Alessia, Lionello, Federico, Salviati, Leonardo, Caminati, Marco, Senna, Gianenrico
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8509830/
https://www.ncbi.nlm.nih.gov/pubmed/34640510
http://dx.doi.org/10.3390/jcm10194493

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8509830/
https://www.ncbi.nlm.nih.gov/pubmed/34640510
http://dx.doi.org/10.3390/jcm10194493

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