Molecular defect of ‘Prothrombin Amrita’: Substitution of arginine by glutamine (Arg553 to Gln) near the Na+ binding loop of prothrombin-Reference-Cited by-同舟云学术

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Molecular defect of ‘Prothrombin Amrita’: Substitution of arginine by glutamine (Arg553 to Gln) near the Na+ binding loop of prothrombin

Published:2013-03 Issue:3 Volume:50 Page:182-183
ISSN:1079-9796
Container-title:Blood Cells, Molecules, and Diseases
language:en
Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Sivasundar Sajini,Oommen Akash Thomas,Prakash Ohm,Baskaran Sujatha,Biswas Raja,Nair Shantikumar,Mohan C. Gopi,Biswas Lalitha

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference6 articles.

1. The A20210 allele of the prothrombin gene is frequently associated with the factor V Arg 506 to Gln mutation but not with protein S deficiency in thrombophilic families;Zoller;Blood,1998

2. Polymorphisms of clotting factors modify the risk for primary intracranial hemorrhage;Corral;Blood,2001

3. Heterozygous for dysprothrombinemia Prothrombin Greenville, Arg517®Gln, identified in an individual heterozygous for dysprothrombinemia;Henriksen;Blood,1998

4. The A20210 allele of the prothrombin gene is frequently associated with the factor V Arg 506 to Gln mutation but not with protein S deficiency in thrombophilic families;Zoller;Blood,1998

5. The Na+ binding site of thrombin;Di Cera;J. Biol. Chem.,1995

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