Diagnosing alpha-1 antitrypsin deficiency: the first step in precision medicine
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DOI: 10.12688/f1000research.12399.1
Abstract: 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… read more here.
Keywords: medicine; precision medicine; deficiency first; alpha antitrypsin ... See more keywords