Cutoff level to detect heterozygous alpha 1 antitrypsin deficiency in Turkish population

Background: Alpha 1 antitrypsin (AT) deficiency is a hereditary disorder leading to the defective defence system against neutrophil elastasis in lung and accumulation of insoluble heterodimer AT molecules in hepatocytes. Knowledge of the prevalence of AT deficiency in each country is important to or...

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Detalhes bibliográficos
Publicado no:J Clin Lab Anal
Main Authors: Simsek, Halis, Pinar, Aslı, Altinbas, Akif, Alp, Alparslan, Balaban, Yasemin H., Buyukasik, Yahya, Ozcebe, Osman, Hascelik, Gulsen, Gedikoglu, Gokhan, Tatar, Gonca
Formato: Artigo
Idioma:Inglês
Publicado em: Wiley Subscription Services, Inc., A Wiley Company 2011
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6647731/
https://ncbi.nlm.nih.gov/pubmed/21786332
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jcla.20472
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