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Molecular diagnosis of alpha1‐antitrypsin deficiency: A new method based on Luminex technology
BACKGROUND: Alpha1‐antitrypsin deficiency (AATD) is an under‐diagnosed hereditary disorder characterized by reduced serum levels of alpha1‐antitrypsin (AAT) and increased risk to develop lung and liver diseases at an early age. AAT is encoded by the highly polymorphic SERPINA1 gene. The most common...
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| Pubblicato in: | J Clin Lab Anal |
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| Autori principali: | , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
John Wiley and Sons Inc.
2020
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7370739/ https://ncbi.nlm.nih.gov/pubmed/32181528 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jcla.23279 |
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