Alpha1-antitrypsin deficiency. 2: genetic aspects of alpha(1)-antitrypsin deficiency: phenotypes and genetic modifiers of emphysema risk.
review · Level V
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- Record sourced from PubMed, PMID 14985567.
- Also identified by PMC identifier 1746953.
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Abstract
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.
Medical subject headings
- Pulmonary Emphysema
- alpha 1-Antitrypsin
- alpha 1-Antitrypsin Deficiency