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The genetics of familial hypercholesterolemia and emerging therapies
Familial hypercholesterolemia (FH) results in very high levels of atherogenic low-density lipoprotein (LDL) cholesterol from the time of birth. Mutations of the genes encoding for the LDL receptor, apolipoprotein B and proprotein convertase subtilisin/kexin type 9, are causes for this autosomal domi...
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| Publicat a: | Appl Clin Genet |
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| Autor principal: | |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Dove Medical Press
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4315461/ https://ncbi.nlm.nih.gov/pubmed/25670911 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/TACG.S44315 |
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