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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Salvato in:
Dettagli Bibliografici
Pubblicato in:J Clin Lab Anal
Autori principali: Ottaviani, Stefania, Barzon, Valentina, Buxens, Amaya, Gorrini, Marina, Larruskain, Amaia, El Hamss, Rachid, Balderacchi, Alice M., Corsico, Angelo G., Ferrarotti, Ilaria
Natura: Artigo
Lingua:Inglês
Pubblicazione: John Wiley and Sons Inc. 2020
Soggetti:
Research Articles
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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