Association Between the G20210A Polymorphism of Prothrombin Gene and Myocardial Infarction in Tunisian Population.

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Mitochondrial Genome Mutations Associated with Myocardial Infarction.

P2860

Q55025572-14EFAE68-B43F-4FE2-9136-E855AD6DBDB2

P2860

Association Between the G20210A Polymorphism of Prothrombin Gene and Myocardial Infarction in Tunisian Population.

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http://www.wikidata.org/entity/Q39116459

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2016 nî lūn-bûn

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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2016年论文

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2016年论文

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name

Association Between the G20210 ...... rction in Tunisian Population.

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Association Between the G20210 ...... rction in Tunisian Population.

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Item

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Association Between the G20210 ...... rction in Tunisian Population.

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Association Between the G20210 ...... rction in Tunisian Population.

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Association Between the G20210 ...... rction in Tunisian Population.

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Association Between the G20210 ...... rction in Tunisian Population.

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P1476

Association Between the G20210 ...... rction in Tunisian Population.

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P2093

Amani Kallel

http://www.w3.org/2001/XMLSchema#string

Mohamed Hedi Sbaï

http://www.w3.org/2001/XMLSchema#string

Mohamed Sami Mourali

http://www.w3.org/2001/XMLSchema#string

Moncef Feki

http://www.w3.org/2001/XMLSchema#string

Naziha Kaabachi

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Rachid Mechmeche

http://www.w3.org/2001/XMLSchema#string

Riadh Jemaa

http://www.w3.org/2001/XMLSchema#string

Yousra Sédiri

http://www.w3.org/2001/XMLSchema#string

P2860

Executive Summary of The Third Report of The National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, And Treatment of High Blood Cholesterol In Adults (Adult Treatment Panel III)

Prothrombin G20210A mutation is associated with young-onset stroke: the genetics of early-onset stroke study and meta-analysis.

Seven haemostatic gene polymorphisms in coronary disease: meta-analysis of 66,155 cases and 91,307 controls.

G20210A prothrombin gene polymorphism and coronary ischaemic syndromes: a phenotype-specific meta-analysis of 12 034 subjects.

Association between factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations and events of the arterial circulatory system: a meta-analysis of published studies.

Epidemiology of Prothrombin G20210A Mutation in the Mediterranean Region.

Endothelial Nitric Oxide Synthase T-786C Mutation, Prothrombin Gene Mutation (G-20210-A) and Protein S Deficiency Could Lead to Myocardial Infarction in a Very Young Male Adult

Cardiovascular disease and heritability of the prothrombotic state.

Arterial thrombus formation in cardiovascular disease.

Lack of association between factor V Leiden and prothrombin G20210A polymorphisms in Tunisian subjects with a history of myocardial infarction.

P2888

s10528-016-9744-y

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653-664

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scholarly article

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10.1007/S10528-016-9744-Y

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27306359

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P921

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Association Between the G20210A Polymorphism of Prothrombin Gene and Myocardial Infarction in Tunisian Population.

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P2860

P2860

Association Between the G20210A Polymorphism of Prothrombin Gene and Myocardial Infarction in Tunisian Population.

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