Augmentation therapy for emphysema due to alpha-1-antitrypsin deficiency
Alpha-1 antitrypsin deficiency (AAT) is a hereditary recessive autosomal disease caused by mutations in the AAT gene. This disease is characterized by abnormally low AAT concentrations in plasma, which, in its homozygote form, carries a high risk for the development of early pulmonary emphysema and...
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| Asıl Yazarlar: | , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
SAGE Publishing
2008-02-01
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| Seri Bilgileri: | Therapeutic Advances in Respiratory Disease |
| Online Erişim: | https://doi.org/10.1177/1753465807088159 |
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