Gly319 → Arg substitution in the dysfunctional prothrombin Segovia

British Journal of Haematology

Volumn 105, Issue 3, 1999, Pages 667-669

  Akhavan, Sepideh ^b   Rocha, Eduardo ^a   Zeinali, Sirous ^b   Mannucci, Pier Mannuccio ^b  

^a UNIVERSITY CLINIC OF NAVARRA   (Spain)

^b NONE

Author keywords

Congenital bleeding disorders; Factor II; Prothrombin

Indexed keywords

AMINO ACID; ARGININE; BLOOD CLOTTING FACTOR 10A; GLYCINE; PROTHROMBIN;

ADULT; AMINO ACID SUBSTITUTION; ARTICLE; BLEEDING; CASE REPORT; DNA SEQUENCE; GENE AMPLIFICATION; GENE SEGREGATION; HOMOZYGOTE; HUMAN; MALE; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN CONFORMATION; PROTEIN DEGRADATION; PROTHROMBIN DEFICIENCY; BLEEDING DISORDER; GENETICS; SINGLE STRAND CONFORMATION POLYMORPHISM;

ADULT; AMINO ACID SUBSTITUTION; HEMORRHAGIC DISORDERS; HUMANS; MALE; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; PROTHROMBIN;

EID: 0033143443     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.1999.01423.x     Document Type: Article

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