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Plasma levels of PCSK9 and phenotypic variability in familial hypercholesterolemia
The extent of hypercholesterolemia varies considerably in patients with familial hypercholesterolemia (FH). We hypothesized that the variability of the FH phenotype might be partly explained by variation in proprotein convertase subtilisin kexin type 9 (PCSK9) activity. Individuals between 18 and 53...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
The American Society for Biochemistry and Molecular Biology
2012
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| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3329397/ https://ncbi.nlm.nih.gov/pubmed/22375030 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1194/jlr.P023994 |
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