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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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| Publicado no: | Int J Chron Obstruct Pulmon Dis |
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| Main Authors: | , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Dove
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6873957/ https://ncbi.nlm.nih.gov/pubmed/31819391 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/COPD.S224221 |
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