Alpha1-antitrypsin (Ξ± 1 AT) deficiency is a hereditary disorder associated with reduced Ξ± 1 AT serum level, predisposing adults to pulmonary emphysema. Among the known mutations of the Ξ± 1 AT gene (SERPINA1) causing Ξ± 1 AT deficiency, a few alleles, particularly the Z allele, may also predispose adu
β¦ LIBER β¦
Molecular mechanisms of alpha1-antitrypsin null alleles
β Scribed by J.H LEE; M BRANTLY
- Book ID
- 117829329
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- English
- Weight
- 249 KB
- Volume
- 94
- Category
- Article
- ISSN
- 0954-6111
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