Diagnosing Alpha-1-Antitrypsin Deficiency Using A PCR/Luminescence-Based Technology

PURPOSE: Alpha-1-antitrypsin deficiency (AATD) is a rare hereditary condition resulting from the mutations in the SERPINA1 (serine protease inhibitor) gene and is characterized by low circulating levels of the alpha-1 antitrypsin (AAT) protein. The traditional algorithm for laboratory testing of AAT...

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Detalles Bibliográficos
Autores principales: Veith, Martina, Klemmer, Andreas, Anton, Iker, El Hamss, Rachid, Rapun, Noelia, Janciauskiene, Sabina, Kotke, Viktor, Herr, Christian, Bals, Robert, Vogelmeier, Claus Franz, Greulich, Timm
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Methodology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6873957/
https://www.ncbi.nlm.nih.gov/pubmed/31819391
http://dx.doi.org/10.2147/COPD.S224221

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6873957/
https://www.ncbi.nlm.nih.gov/pubmed/31819391
http://dx.doi.org/10.2147/COPD.S224221

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