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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...
Gardado en:
| Publicado en: | Int J Chron Obstruct Pulmon Dis |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Dove
2020
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| Assuntos: | |
| Acceso en liña: | 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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