Polymorphism of thrombin-activatable fibrinolysis inhibitor and risk of intracranial haemorrhage in factor XIII deficiency

Haemophilia

Volumn 20, Issue 1, 2014, Pages

  Naderi, M ^a   Dorgalaleh, A ^b   Alizadeh, S ^b   Kashani Khatib, Z ^b   Tabibian, S ^b   Kazemi, A ^b   Dargahi, H ^b   Bamedi, T ^a  

^a ZAHEDAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^b TEHRAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CLOTTING FACTOR 13 DEFICIENCY; BLOOD CLOTTING FACTOR 13 GENE; BRAIN HEMORRHAGE; CASE CONTROL STUDY; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; GENE; GENETIC POLYMORPHISM; HUMAN; LETTER; MALE; PRIORITY JOURNAL; RISK FACTOR;

CARBOXYPEPTIDASE U; CASE-CONTROL STUDIES; FACTOR XIII DEFICIENCY; FEMALE; HETEROZYGOTE; HOMOZYGOTE; HUMANS; INTRACRANIAL HEMORRHAGES; MALE; ODDS RATIO; POLYMORPHISM, GENETIC;

EID: 84890860409     PISSN: 13518216     EISSN: 13652516     Source Type: Journal    
DOI: 10.1111/hae.12287     Document Type: Letter

References (10)

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