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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Sharp, Richard R, de Serres, Frederick, Newman, Lee, Sandhaus, Robert A, Walsh, John W, Hood, Ernie, Harry, G Jean
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2003
Pynciau:
Research Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC1241718/
https://ncbi.nlm.nih.gov/pubmed/14594626
Tagiau: Ychwanegu Tag
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