Real world evaluation of a novel lateral flow assay (AlphaKit® QuickScreen) for the detection of alpha-1-antitrypsin deficiency

BACKGROUND: Alpha-1-Antitrypsin (AAT) deficiency (AATD) is a hereditary disorder that manifests primarily as pulmonary emphysema and liver cirrhosis. The clinically most relevant mutation causing AATD is a single nucleotide polymorphism Glu342Lys (Z-mutation). Despite the recommendation to test ever...

Descripción completa

Detalles Bibliográficos
Autores principales: Greulich, Timm, Rodríguez-Frias, Francisco, Belmonte, Irene, Klemmer, Andreas, Vogelmeier, Claus F., Miravitlles, Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6090649/
https://www.ncbi.nlm.nih.gov/pubmed/30103740
http://dx.doi.org/10.1186/s12931-018-0826-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6090649/
https://www.ncbi.nlm.nih.gov/pubmed/30103740
http://dx.doi.org/10.1186/s12931-018-0826-8

Ejemplares similares