Alpha-1 antitrypsin deficiency: outstanding questions and future directions

BACKGROUND: Alpha-1 antitrypsin deficiency (AATD) is a rare hereditary condition that leads to decreased circulating alpha-1 antitrypsin (AAT) levels, significantly increasing the risk of serious lung and/or liver disease in children and adults, in which some aspects remain unresolved. METHODS: In t...

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Detalles Bibliográficos
Autores principales: Torres-Durán, María, Lopez-Campos, José Luis, Barrecheguren, Miriam, Miravitlles, Marc, Martinez-Delgado, Beatriz, Castillo, Silvia, Escribano, Amparo, Baloira, Adolfo, Navarro-Garcia, María Mercedes, Pellicer, Daniel, Bañuls, Lucía, Magallón, María, Casas, Francisco, Dasí, Francisco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6042212/
https://www.ncbi.nlm.nih.gov/pubmed/29996870
http://dx.doi.org/10.1186/s13023-018-0856-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6042212/
https://www.ncbi.nlm.nih.gov/pubmed/29996870
http://dx.doi.org/10.1186/s13023-018-0856-9

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