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α1-Antitrypsin deficiency•2:: Genetic aspects of α1-antitrypsin deficiency:: phenotypes and genetic modifiers of emphysema risk

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THORAX
卷 59, 期 3, 页码 259-264

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BMJ PUBLISHING GROUP
DOI: 10.1136/thx.2003.006502

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  1. NHLBI NIH HHS [R01HL68926, K08 HL072918] Funding Source: Medline

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The genetic aspects of AAT deficiency and the variable manifestations of lung disease in PI Z individuals are reviewed. The role of modifying genetic factors which may interact with environmental factors (such as cigarette smoking) is discussed, and directions for future research are presented.

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