000 01175 a2200373 4500
005 20250513211705.0
264 0 _c20000905
008 200009s 0 0 eng d
022 _a0340-6245
040 _aNLM
_beng
_cNLM
100 1 _aCoulet, F
245 0 0 _aLack of association of the prothrombin gene variant G20210A with myocardial infarction in Caucasian males.
_h[electronic resource]
260 _bThrombosis and haemostasis
_cMay 2000
300 _a796-7 p.
_bdigital
500 _aPublication Type: Letter; Multicenter Study
650 0 4 _a3' Untranslated Regions
_xgenetics
650 0 4 _aAdult
650 0 4 _aAlleles
650 0 4 _aDNA Mutational Analysis
650 0 4 _aEurope
_xepidemiology
650 0 4 _aGene Frequency
650 0 4 _aGenetic Predisposition to Disease
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aMyocardial Infarction
_xepidemiology
650 0 4 _aProthrombin
_xgenetics
650 0 4 _aRisk Factors
650 0 4 _aWhite People
_xgenetics
700 1 _aGodard, V
700 1 _aVerdy, E
700 1 _aSoubrier, F
773 0 _tThrombosis and haemostasis
_gvol. 83
_gno. 5
_gp. 796-7
999 _c10774884
_d10774884