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Homozygous Familial Hypercholesterolemia: Case Series and Review of the Literature
Introduction. Familial hypercholesterolemia (FH) is caused by nonfunctioning low-density lipoprotein (LDL) receptors, resulting in high serum cholesterol. Two types of FH are described: the heterozygous form is diagnosed in adults and responds well to medical therapy; the homozygous form is rare, di...
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| Päätekijät: | , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Hindawi Publishing Corporation
2011
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3505937/ https://ncbi.nlm.nih.gov/pubmed/23213598 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2011/154908 |
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