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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Publicado en:Eur Respir J
Autores principales: McElvaney, Gerard N., Sandhaus, Robert A., Miravitlles, Marc, Turino, Gerard M., Seersholm, Niels, Wencker, Marion, Stockley, Robert A.
Formato: Artigo
Lenguaje:Inglês
Publicado: European Respiratory Society 2020
Materias:
Reviews
Acceso en línea: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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