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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...
Sparad:
| I publikationen: | Appl Clin Genet |
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| Huvudupphovsman: | |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Dove Medical Press
2015
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| Ämnen: | |
| Länkar: | 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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