Differential DNA methylation in familial hypercholesterolemia

BACKGROUND: Familial hypercholesterolemia (FH) is a monogenic disorder characterized by elevated low-density lipoprotein cholesterol (LDL-C). A FH causing genetic variant in LDLR, APOB, or PCSK9 is not identified in 12–60% of clinical FH patients (FH mutation-negative patients). We aimed to assess w...

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Detalhes bibliográficos
Publicado no:EBioMedicine
Main Authors: Reeskamp, Laurens F., Venema, Andrea, Pereira, Joao P.Belo, Levin, Evgeni, Nieuwdorp, Max, Groen, Albert K., Defesche, Joep C., Grefhorst, Aldo, Henneman, Peter, Hovingh, G.Kees
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2020
Assuntos:
Research Paper
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7581877/
https://ncbi.nlm.nih.gov/pubmed/33096472
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ebiom.2020.103079
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