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Role of alpha-1-antichymotrypsin deficiency in promoting cirrhosis in two siblings with heterozygous alpha-1-antitrypsin deficiency phenotype SZ

Background: Alpha-1-antitrypsin (A1AT) deficiency is the most common inherited metabolic disorder with the potential to cause injury in the lung and liver. Recent reports suggested that alpha-1-antichymotrypsin (A1AC) deficiency may also be a possible cause of chronic liver disease. However, it has...

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Autors principals: Yoon, D, Kueppers, F, Genta, R M, Klintmalm, G B, Khaoustov, V I, Yoffe, B
Format: Artigo
Idioma:Inglês
Publicat: Copyright 2002 by Gut 2002
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC1773188/
https://ncbi.nlm.nih.gov/pubmed/11950825
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