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        Thromb Haemost 1996; 76(02): 277-278
DOI: 10.1055/s-0038-1650570
   DOI: 10.1055/s-0038-1650570
Letters to the Editor
   Prenatal Diagnosis of Compound Heterozygous Deficiency of Protein C by Direct Detection of the Mutation Sites
Authors
Further Information
            
               
                  
            
         
      
   Publication History
Received 01 March 1996
Accepted after resubmission 15 April 1996
Publication Date:
10 July 2018 (online)
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References
 - 1 Suzuki K. Protein C. In: Molecular Basis of Thrombosis and Hemostasis High KA, Roberts H. eds. Marcel Dekker, Inc.; New York: 1995: 393-424
 - 2 Ido M, Ohiwa M, Hayashi T, Nishioka J, Hatada T, Watanabe Y, Wada H, Shirakawa S, Suzuki K. A compound heterozygous protein C deficiency with a single nucleotide G deletion encoding Gly-381 and an amino acid substitution of Lys for Gla-26. Thromb Haemost 1993; 70: 636-641
 - 3 Nishioka J, Ido M, Hayashi T, Suzuki K. The Gla26 residue of protein C is required for the binding of thrombomodulin and endothelial cell protein C receptor, but not to protein S and factor Va. Thromb Haemost 1996; 75: 275-282