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Improving the Lives of Patients with Alpha-1 Antitrypsin Deficiency
Alpha-1 Antitrypsin Deficiency (AATD) is a rare genetic condition that predisposes patients to lung and liver disease and is often underdiagnosed due to incomplete diagnosis of chronic obstructive pulmonary disease (COPD) and asthma. Improvements in physician awareness have been made, but better str...
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| Vydáno v: | Int J Chron Obstruct Pulmon Dis |
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| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Dove
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7735792/ https://ncbi.nlm.nih.gov/pubmed/33328731 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/COPD.S276773 |
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