Title of article :
α1-antitrypsin deficiency
Author/Authors :
James K. Stoller، نويسنده , , Loutfi S. Aboussouan، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2005
Abstract :
α1-antitrypsin deficiency is a genetic disorder that affects about one in 2000–5000 individuals. It is clinically characterised by liver disease and early-onset emphysema. Although α1 antitrypsin is mainly produced in the liver, its main function is to pr
Journal title :
The Lancet
Journal title :
The Lancet