THE CO-EXSISTANCE OF β-FIBRINOGEN -455 G/A POLYMORPHISM AND PROTHROMBIN 20210 G/A MUTATION IN CORONARY HEART DISEASE IN EGYPTIAN PATIENTS

Mohamed Shehata Ali;

Abstract


Coronary Heart Disease (CHD) is a complex disease with both environmental
and genetic determinants. The aim of this study was to assess the presence of FGB-
455 G/A and prothrombin 20210 G/A polymorphisms in CHD Egyptian patients
and to correlate the c

Other data

Title THE CO-EXSISTANCE OF β-FIBRINOGEN -455 G/A POLYMORPHISM AND PROTHROMBIN 20210 G/A MUTATION IN CORONARY HEART DISEASE IN EGYPTIAN PATIENTS
Other Titles اقتران وجود طفرتى فيبرينوجين بيتا-455ج/أ وبروثرومبين 20210 ج/أ فى مرضى الشرايين التاجية المصريين
Authors Mohamed Shehata Ali
Keywords THE CO-EXSISTANCE OF β-FIBRINOGEN -455 G/A POLYMORPHISM AND PROTHROMBIN 20210 G/A MUTATION IN CORONARY HEART DISEASE IN EGYPTIAN PATIENTS
Issue Date 2010
Description 
Coronary Heart Disease (CHD) is a complex disease with both environmental
and genetic determinants. The aim of this study was to assess the presence of FGB-
455 G/A and prothrombin 20210 G/A polymorphisms in CHD Egyptian patients
and to correlate the c

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