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...

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Detalles Bibliográficos
Autores principales: Schneider, Carolin V., Strnad, Pavel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2021
Materias:
Original Research
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

Internet

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

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