Monocytes and Macrophages in Alpha-1 Antitrypsin Deficiency

Alpha-1 antitrypsin deficiency (AATD) is a genetic condition characterised by low circulating levels of alpha-1 antitrypsin (AAT), a serine proteinase inhibitor. The most common deficiency variants are the S and Z mutations, which cause the accumulation of misfolded AAT in hepatocytes resulting in e...

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Detalles Bibliográficos
Autores principales: Belchamber, Kylie B R, Walker, Eloise M, Stockley, Robert A, Sapey, Elizabeth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7725100/
https://www.ncbi.nlm.nih.gov/pubmed/33311976
http://dx.doi.org/10.2147/COPD.S276792

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7725100/
https://www.ncbi.nlm.nih.gov/pubmed/33311976
http://dx.doi.org/10.2147/COPD.S276792

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