Familial apolipoprotein E deficiency.
A unique kindred with premature cardiovascular disease, tubo-eruptive xanthomas, and type III hyperlipoproteinemia (HLP) associated with familial apolipoprotein (apo) E deficiency was examined. Homozygotes (n = 4) had marked increases in cholesterol-rich very low density lipoproteins (VLDL) and inte...
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| Udgivet i: | J Clin Invest |
|---|---|
| Principais autores: | , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
American Society for Clinical Investigation
1986
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC423806/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3771793/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI112704 |
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