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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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Sonraí Bibleagrafaíochta
Main Authors: Sharp, Richard R, de Serres, Frederick, Newman, Lee, Sandhaus, Robert A, Walsh, John W, Hood, Ernie, Harry, G Jean
Formáid: Artigo
Teanga:Inglês
Foilsithe: 2003
Ábhair:
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC1241718/
https://ncbi.nlm.nih.gov/pubmed/14594626
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