Environmental, occupational, and genetic risk factors for alpha-1 antitrypsin deficiency.

Alpha-1 antitrypsin (AAT) deficiency is an inherited genetic disorder currently diagnosed in approximately 5,000 people in the United States. Although some individuals with AAT deficiency are asymptomatic, the condition often leads to deterioration of lung function in adults and is associated with e...

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Detalhes bibliográficos
Main Authors: Sharp, Richard R, de Serres, Frederick, Newman, Lee, Sandhaus, Robert A, Walsh, John W, Hood, Ernie, Harry, G Jean
Formato: Artigo
Idioma:Inglês
Publicado em: 2003
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1241718/
https://ncbi.nlm.nih.gov/pubmed/14594626
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