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   Hereditary of Alpha-1-Antitrypsin Deficiency  
   
نویسنده Gholami Sara ,Hamzehloei Tayebeh
منبع shiraz e-medical journal - 2013 - دوره : 14 - شماره : 1 - صفحه:63 -75
چکیده    In this review article, in addition to the clinical manifestation of the alpha 1 antitryp-sin deficiency, the genetics and molecular diagnosis of the disease and the effects of the causative mutations were reviewed.
کلیدواژه Alpha 1 antitrypsin deficiency ,Pi ZZ ,Molecular diagnosis of AATD
آدرس mashhad university of medical sciences, ایران, mashhad university of medical sciences, ایران
پست الکترونیکی hamzehloiet@mums.ac.ir
 
     
   
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