Homozygous G20210A transition in the prothrombin gene associated with severe venous thrombotic disease: Two cases in a French family [1]

Thrombosis and Haemostasis

Volumn 80, Issue 6, 1998, Pages 1027-1028

  Zawadzki, C ^a   Gaveriaux, V ^a   Trillot, N ^a   Bauters, A ^a   Watel, A ^a   Alhenc Gelas, M ^a   Preudhomme, C ^a   Jude, B ^a  

^a LILLE UNIVERSITY HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIVITAMIN K; PROTHROMBIN;

ADULT; AGED; CLINICAL ARTICLE; DEEP VEIN THROMBOSIS; FEMALE; GENE MAPPING; GENE MUTATION; GENETIC RISK; GENOTYPE; HETEROZYGOTE; HOMOZYGOTE; HUMAN; LETTER; MALE; PEDIGREE; PRIORITY JOURNAL;

EID: 0031732779     PISSN: 03406245     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0037-1615406     Document Type: Letter

References (10)