Thrombophilic gene polymorphism studies in G6PD deficient individuals from Saudi population

We performed a study to evaluate the role of three single nucleotide polymorphisms (SNPs), factor V Leiden G1691A (FVL), prothrombin gene mutation G20210A (PRT or FII-G20210A) and methylenotetrahydrofolate reductase variant C677T (MTHFRC677T), as risk factors for G6PD in Saudi populations. Our resul...

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Detalles Bibliográficos
Autores principales: Alharbi, Khalid K, Khan, Imran Ali, Syed, Rabbani
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Biomedical Informatics 2012
Materias:
Hypothesis
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3532010/
https://www.ncbi.nlm.nih.gov/pubmed/23275730
http://dx.doi.org/10.6026/97320630081255

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3532010/
https://www.ncbi.nlm.nih.gov/pubmed/23275730
http://dx.doi.org/10.6026/97320630081255

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