Author:
Ortega Luis,Balboa Florencio,González Lucía
Subject
Pediatrics, Perinatology, and Child Health
Reference10 articles.
1. The microheterogeneity of desialylated α1-antichymotrypsin: The occurrence of two amino-terminal isoforms, one lacking a His-Pro dipeptide;Lindmark;Biochim. Biophys. Acta,1989
2. Partial deficiency of α1-antichymotrypsin is associated with chronic cryptogenic liver disease;Lindmark;Scand. J. Gastroenterol,1991
3. A kinetic mechanism for the polymerization of α1-antitrypsin;Dafforn;J. Biol. Chem,1999
4. A 370-kb cosmid contig of the serpin gene cluster on human chromosome 14q32.1: Molecular linkage of the genes encoding alpha 1-antichymotrypsin, protein C inhibitor, kallistatin, α1-antitrypsin, and corticosteroid- binding globulin;Rollini;Genomics,1997
5. Familiar α1-antichymotrypsin deficiency;Eriksson;Acta Med. Scand,1986
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