Screening of common genetic variants in the APOB gene related to familial hypercholesterolemia in a Saudi population: A case–control study

Familial hypercholesterolemia (FH) is a monogenic dominant inherited disorder of lipid metabolism characterized by elevated low-density lipoprotein levels, and is mainly attributable to mutations in low-density lipoprotein receptor (LDLR), apolipoprotein B (APOB), and proportein convertase subtilisi...

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Detalles Bibliográficos
Autores principales: Batais, Mohammed Ali, Almigbal, Turky H., Shaik, Noor Ahmad, Alharbi, Fawaziah Khalaf, Alharbi, Khalid Khalaf, Ali Khan, Imran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6358331/
https://www.ncbi.nlm.nih.gov/pubmed/30681615
http://dx.doi.org/10.1097/MD.0000000000014247

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6358331/
https://www.ncbi.nlm.nih.gov/pubmed/30681615
http://dx.doi.org/10.1097/MD.0000000000014247

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