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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Detalles Bibliográficos
Autores principales: Alharbi, Khalid Khalaf, Alnbaheen, May Salem, Alharbi, Fawiziah Khalaf, Hasanato, Rana M., Khan, Imran Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: King Faisal Specialist Hospital and Research Centre 2017
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6074118/
https://www.ncbi.nlm.nih.gov/pubmed/29229890
http://dx.doi.org/10.5144/0256-4947.2017.425

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6074118/
https://www.ncbi.nlm.nih.gov/pubmed/29229890
http://dx.doi.org/10.5144/0256-4947.2017.425

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