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Q192R polymorphism in the PON1 gene and familial hypercholesterolemia in a Saudi population
BACKGROUND: Familial hypercholesterolemia (FH) is an autosomal dominant condition characterized by abnormal levels of low-density lipoprotein (LDL) in the blood. FH is a risk factor for atherosclerosis and cardiovascular disease. The relationship between the paraoxonase 1 (PON1) gene, atherosclerosi...
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| Publicado en: | Ann Saudi Med |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
King Faisal Specialist Hospital and Research Centre
2017
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6074118/ https://ncbi.nlm.nih.gov/pubmed/29229890 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5144/0256-4947.2017.425 |
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