Association of the platelet glycoprotein Ia C807T/G873A gene polymorphism and thrombosis in behçet patients

Haematologia

Volumn 32, Issue 2, 2002, Pages 121-128

  Polat, Gürbz ^a   Eskandari, Gülçin ^a   Kaya, Tamer Irfan ^a   Türsen, Ümit ^a   Bagdatoglu, Özlen ^a   Ikizoglu, Güliz ^a   Atik, Ugur ^a  

^a MERSIN UNIVERSITY   (Turkey)

Author keywords

Beh et's disease; Glycoprotein; Platelet; Polymorphism; Thrombus

Indexed keywords

FIBRINOGEN RECEPTOR; GENOMIC DNA; VERY LATE ACTIVATION ANTIGEN 2;

ALLELE; ARTICLE; BEHCET DISEASE; CLINICAL ARTICLE; CONFIDENCE INTERVAL; CONTROLLED STUDY; DNA POLYMORPHISM; GENETIC LINKAGE; GENOTYPE; HUMAN; POLYMERASE CHAIN REACTION; PREVALENCE; RISK FACTOR; TURKEY (REPUBLIC); VEIN THROMBOSIS;

BEHCET SYNDROME; CASE-CONTROL STUDIES; GENE FREQUENCY; GENOTYPE; HUMANS; INTEGRIN ALPHA2; LINKAGE (GENETICS); ODDS RATIO; POINT MUTATION; POLYMORPHISM, GENETIC; THROMBOSIS; TURKEY;

EID: 0036903692     PISSN: 00176559     EISSN: None     Source Type: Journal    
DOI: 10.1163/156855902320387952     Document Type: Article

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