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Diagnosing alpha-1 antitrypsin deficiency: the first step in precision medicine
Severe alpha-1 antitrypsin (AAT) deficiency is one of the most common serious genetic diseases in adults of European descent. Individuals with AAT deficiency have a greatly increased risk for emphysema and liver disease. Other manifestations include bronchiectasis, necrotizing panniculitis and granu...
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| Publicado no: | F1000Res |
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| Autor principal: | |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
F1000 Research Limited
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5710307/ https://ncbi.nlm.nih.gov/pubmed/29225784 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12688/f1000research.12399.1 |
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