Genetic variants of alpha-1-antitrypsin (AAT)
Author:
Publisher
Wiley
Subject
Hepatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0676.1992.tb01064.x/fullpdf
Reference31 articles.
1. Molecular basis of alpha-1-antitrypsin deficiency;Brantly;Am J Med,1988
2. Characterization of the M1 (Ala 213) type of alpha-1-antitrypsin, a newly recognized common “normal” alpha-1-antitrypsin haplo-type;Nukiwa;Biochemistry,1987
3. Characterization of the gene and protein of the common, alpha-1-antitrypsin normal M2 allele;Nukiwa;Am J Hum Genet,1988
4. Alpha-1-antitrypsin Christ-church, 363 Glu-Lys mutation at the P'5 position does not affect inhibitory activity;Brennan;Biochim Biophys Acta,1986
5. The amino acid substitutions of human alpha-1-antitrypsin M3, X and Z;Jeppsson;FEBS Lett,1988
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