Genetic polymorphisms in paraoxonase 1 and G protein-coupled receptor 77, and the risk of glucose-6-phosphate dehydrogenase deficiency in a Saudi population

OBJECTIVES: To investigate the role of amino acid substitution variants Q192R and C698T in the development of glucose-6-phosphate dehydrogenase (G6PD) deficiency in a Saudi male population. METHODS: This case-control study was carried out in 200 Saudi male individuals: 100 patients with G6PD deficie...

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Detalles Bibliográficos
Autor principal: Alharbi, Khalid K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Saudi Medical Journal 2015
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4436749/
https://www.ncbi.nlm.nih.gov/pubmed/25935173
http://dx.doi.org/10.15537/smj.2015.5.11860

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4436749/
https://www.ncbi.nlm.nih.gov/pubmed/25935173
http://dx.doi.org/10.15537/smj.2015.5.11860

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