Title of article
α1-antitrypsin deficiency
Author/Authors
James K. Stoller، نويسنده , , Loutfi S. Aboussouan، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2005
Pages
12
From page
2225
To page
2236
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
Serial Year
2005
Journal title
The Lancet
Record number
588280
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