Multiplex Protein Biomarker Profiling in Patients with Familial Hypercholesterolemia

Familial hypercholesterolemia (FH), is an autosomal dominant disorder caused by mutations in the LDLR, APOB, PCSK9, and APOE genes and is characterized by high plasma levels of total and low-density lipoprotein (LDL) cholesterol. Our study aimed to analyze the influences of two different therapies o...

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Detalles Bibliográficos
Autores principales: Dlouha, Dana, Blaha, Milan, Rohlova, Eva, Hubacek, Jaroslav A., Lanska, Vera, Visek, Jakub, Blaha, Vladimir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8535274/
https://www.ncbi.nlm.nih.gov/pubmed/34680994
http://dx.doi.org/10.3390/genes12101599

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8535274/
https://www.ncbi.nlm.nih.gov/pubmed/34680994
http://dx.doi.org/10.3390/genes12101599

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