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Article

Association of venous thromboembolism and myocardial infarction with Factor V Leiden and Factor II gene mutations among Libyan patients.

The Libyan journal of medicine - 1 Dec 2021

Msalati Abdulghani, Bashein Abdulla, Ghrew Murad, Khalil Ibtesam, Sedaa Khaled, Ali Abushawashi, Zaid Ahmed

Abstract excerpt

Factor V Leiden G1691A (FVL) and Factor II prothrombin G20210A (PGM) mutations are the leading causes of thrombophilia. In this study, we have investigated the prevalence of the FVL G1691A and PGM G20210A single nucleotide polymorphisms (SNPs) among Libyan deep vein thrombosis (DVT) and myocardial infarction (MI) patients. SNP genotyping was performed using high-resolution melt analysis (HRM) and DNA sequencing....

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Share to Factor V
Share to Genetic Predisposition to Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Polymorphism, Single Nucleotide

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Source

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Identifiers

PMID: 33470184
DOI: 10.1080/19932820.2020.1857525
PMCID: PMC7833017

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