The prothrombin 20210 a allele is frequently coinherited in young carriers of the factor V Arg 506 to Gln mutation with venous thrombophilia [2]

Blood

Volumn 91, Issue 6, 1998, Pages 2209-2210

  Ehrenforth, S ^a   Ludwig, G ^a   Klinke, S ^a   Krause, M ^a   Scharrer, I ^a   Nowak Gottl, U ^a  

^a UNIVERSITY HOSPITAL FRANKFURT   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ACTIVATED PROTEIN C; ARGININE; BLOOD CLOTTING FACTOR 5; GENE PRODUCT; GLUTAMINE; PROTHROMBIN;

ADULT; ALLELE; AMINO ACID SUBSTITUTION; CONTROLLED STUDY; FEMALE; GENE FREQUENCY; GENE MUTATION; GENETIC RISK; GENOTYPE; HEMOSTASIS; HOMOZYGOSITY; HUMAN; LETTER; MAJOR CLINICAL STUDY; MALE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; THROMBOPHILIA; VEIN THROMBOSIS;

EID: 0032521209     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v91.6.2209     Document Type: Letter

References (20)