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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Publicat a:J Clin Lab Anal
Autors principals: Ottaviani, Stefania, Barzon, Valentina, Buxens, Amaya, Gorrini, Marina, Larruskain, Amaia, El Hamss, Rachid, Balderacchi, Alice M., Corsico, Angelo G., Ferrarotti, Ilaria
Format: Artigo
Idioma:Inglês
Publicat: John Wiley and Sons Inc. 2020
Matèries:
Research Articles
Accés en línia: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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