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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Detalles Bibliográficos
Autores principales: Sharp, Richard R, de Serres, Frederick, Newman, Lee, Sandhaus, Robert A, Walsh, John W, Hood, Ernie, Harry, G Jean
Formato: Texto
Lenguaje:English
Publicado: 2003
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1241718/
https://www.ncbi.nlm.nih.gov/pubmed/14594626

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1241718/
https://www.ncbi.nlm.nih.gov/pubmed/14594626

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