Diagnosis of alpha1-antitrypsin deficiency not just in severe COPD
Alpha1-antitrypsin deficiency (AATD) is a well known genetic risk factor for pulmonary disease and is the most frequent hereditary disease diagnosed in adults. Despite being one of the most common hereditary diseases, AATD remains under-diagnosed because of its variable clinical presentation and the...
| Asıl Yazarlar: | , , , , |
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| Materyal Türü: | Makale |
| Dil: | English |
| Baskı/Yayın Bilgisi: |
Taylor & Francis
2018-11-01
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| Seri Bilgileri: | Pulmonology |
| Online Erişim: | http://www.sciencedirect.com/science/article/pii/S2531043718300813 |