The Ala25-Thr mutation in the thrombomodulin gene is not frequent in Swedish patients suffering from ischemic heart disease [9]

Thrombosis and Haemostasis

Volumn 82, Issue 4, 1999, Pages 1367-1368

  Norlund, L ^a   Holm, J ^a   Zoller, B ^a   Ohlin, A K ^a  

^a LUND UNIVERSITY HOSPITAL   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

THROMBOMODULIN; ALANINE; THREONINE;

ADULT; AGED; FEMALE; GENE FREQUENCY; GENE MUTATION; HUMAN; ISCHEMIC HEART DISEASE; LETTER; MAJOR CLINICAL STUDY; MALE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM; SWEDEN; GENETICS; HEART MUSCLE ISCHEMIA; MIDDLE AGED; POINT MUTATION;

ADULT; AGED; AGED, 80 AND OVER; ALANINE; FEMALE; GENE FREQUENCY; HUMANS; MALE; MIDDLE AGED; MYOCARDIAL ISCHEMIA; POINT MUTATION; SWEDEN; THREONINE; THROMBOMODULIN;

EID: 0032589781     PISSN: 03406245     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0037-1614398     Document Type: Letter

References (9)