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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Detaylı Bibliyografya
Yayımlandı:J Clin Lab Anal
Asıl Yazarlar: Simsek, Halis, Pinar, Aslı, Altinbas, Akif, Alp, Alparslan, Balaban, Yasemin H., Buyukasik, Yahya, Ozcebe, Osman, Hascelik, Gulsen, Gedikoglu, Gokhan, Tatar, Gonca
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Wiley Subscription Services, Inc., A Wiley Company 2011
Konular:
Original Articles
Online Erişim: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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