Results from a large targeted screening program for alpha-1-antitrypsin deficiency: 2003 - 2015

BACKGROUND: Alpha-1-antitrypsin deficiency (AATD) is an autosomal codominant inherited disease that is significantly underdiagnosed. We have previously shown that the combination of an awareness campaign with the offer of free diagnostic testing results in the detection of a relevant number of sever...

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Detalles Bibliográficos
Autores principales: Greulich, Timm, Nell, Christoph, Herr, Christian, Vogelmeier, Claus, Kotke, Viktor, Wiedmann, Stefan, Wencker, Marion, Bals, Robert, Koczulla, Andreas Rembert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4901499/
https://www.ncbi.nlm.nih.gov/pubmed/27282198
http://dx.doi.org/10.1186/s13023-016-0453-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4901499/
https://www.ncbi.nlm.nih.gov/pubmed/27282198
http://dx.doi.org/10.1186/s13023-016-0453-8

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