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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Detalhes bibliográficos
Publicado no:J Clin Lab Anal
Main Authors: Ottaviani, Stefania, Barzon, Valentina, Buxens, Amaya, Gorrini, Marina, Larruskain, Amaia, El Hamss, Rachid, Balderacchi, Alice M., Corsico, Angelo G., Ferrarotti, Ilaria
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2020
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Research Articles
Acesso em linha: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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