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...

Descripción completa

Detalles Bibliográficos
Autores principales: McElvaney, Gerard N., Sandhaus, Robert A., Miravitlles, Marc, Turino, Gerard M., Seersholm, Niels, Wencker, Marion, Stockley, Robert A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2020
Materias:
Reviews
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7301289/
https://www.ncbi.nlm.nih.gov/pubmed/32165400
http://dx.doi.org/10.1183/13993003.02410-2019

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7301289/
https://www.ncbi.nlm.nih.gov/pubmed/32165400
http://dx.doi.org/10.1183/13993003.02410-2019

Ejemplares similares