Genetics of Familial Hypercholesterolemia: New Insights

Familial hypercholesterolemia (FH) is one of the most common monogenic diseases, leading to an increased risk of premature atherosclerosis and its cardiovascular complications due to its effect on plasma cholesterol levels. Variants of three genes (LDL-R, APOB and PCSK9) are the major causes of FH,...

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Detalles Bibliográficos
Autores principales: Vrablik, Michal, Tichý, Lukas, Freiberger, Tomas, Blaha, Vladimir, Satny, Martin, Hubacek, Jaroslav A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7575810/
https://www.ncbi.nlm.nih.gov/pubmed/33133164
http://dx.doi.org/10.3389/fgene.2020.574474

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7575810/
https://www.ncbi.nlm.nih.gov/pubmed/33133164
http://dx.doi.org/10.3389/fgene.2020.574474

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