High Prevalence of MTHFR GeneA1298CPolymorphism in Lebanon-Reference-Cited by-同舟云学术

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High Prevalence of MTHFR GeneA1298CPolymorphism in Lebanon

Published:2008-03 Issue:1 Volume:12 Page:75-80
ISSN:1090-6576
Container-title:Genetic Testing
language:en
Short-container-title:Genetic Testing

Author:

Sabbagh Amira S.¹,Mahfoud Ziyad²,Taher Ali³,Zaatari Ghazi¹,Daher Rose¹,Mahfouz Rami A.R.¹

Affiliation:

1. Department of Pathology and Laboratory Medicine, American University of Beirut Medical Center, Beirut, Lebanon.

2. Department of Epidemiology and Population Health, American University of Beirut Medical Center, Beirut, Lebanon.

3. Department of Internal Medicine, American University of Beirut Medical Center, Beirut, Lebanon.

Publisher

Mary Ann Liebert Inc

Subject

Genetics(clinical)

Link

http://www.liebertpub.com/doi/pdf/10.1089/gte.2007.0064

Reference55 articles.

1. A common mutation in 5,10-methylenetetrahydrofolate reductase (MTHFR) gene in two Arab communities

2. C677T and A1298C single nucleotide polymorphisms in the methylenetetrahydrofolate reductase gene among Bahraini Arabs

3. Differences in the frequency of the C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene among the Lebanese population

4. Prevalence of MTHFR gene polymorphisms (C677T and A1298C) among Tamilians

5. Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in a Greek population of blood donors

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1. KASP-PCR method to screen thrombophilia genetic risk factors;2023-10-25

2. Prevalence of MTHFR Gene (C677T and A1298C) Polymorphism in the Syrian Coastal Area;Research Journal of Pharmacy and Technology;2023-09-30

3. MTHFR A1298C polymorphism: a predictor of reduced risk of preeclampsia in Punjab, Pakistan;Hypertension in Pregnancy;2023-03-15

4. Prevalence of thrombophilia-associated mutations and their clinical significance in a large cohort of Lebanese patients;Meta Gene;2021-09

5. An Unusual Case of Concurrent Central Retinal Vein and Cilioretinal Artery Occlusion in a Healthy Patient;Case Reports in Ophthalmology;2021-05-10

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