Cargando...

α(1)-Antitrypsin deficiency · 6: New and emerging treatments for α(1)-antitrypsin deficiency

Alpha-1-antitrypsin (AAT) deficiency is a genetic condition that increases the risk of developing lung and liver disease, as well as other associated conditions. Most treatment of affected individuals is not specifically directed at AAT deficiency but focuses on the resultant disease state. The only...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autor principal: Sandhaus, R
Formato: Artigo
Lenguaje:Inglês
Publicado: BMJ Group 2004
Materias:
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC1746849/
https://ncbi.nlm.nih.gov/pubmed/15454659
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/thx.2003.006551
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!