Future Perspectives in the Diagnosis and Treatment of Liver Disease Associated with Alpha-1 Antitrypsin Deficiency

Alpha-1 antitrypsin deficiency (AATD) is one of the most common genetic diseases and is caused by mutations in the SERPINA1 gene. The homozygous Pi*Z variant is responsible for the majority of the classic severe form of alpha-1 antitrypsin deficiency, which is characterized by markedly decreased lev...

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Detalles Bibliográficos
Autores principales: Abreu, Nélia, Pereira, Vítor Magno, Pestana, Madalena, Jasmins, Luís
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2023
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10586215/
https://www.ncbi.nlm.nih.gov/pubmed/37868641
http://dx.doi.org/10.1159/000528809

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10586215/
https://www.ncbi.nlm.nih.gov/pubmed/37868641
http://dx.doi.org/10.1159/000528809

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