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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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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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F1000 Research Limited
2017
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5710307/ https://www.ncbi.nlm.nih.gov/pubmed/29225784 http://dx.doi.org/10.12688/f1000research.12399.1 |